# Electronic Supplementary Material (ESI) for Organic Chemistry Frontiers.
# This journal is © the Partner Organisations 2023

####################################################################### 
# 
# This file contains crystal structure data downloaded from the 
# Cambridge Structural Database (CSD) hosted by the Cambridge 
# Crystallographic Data Centre (CCDC).
# 
# Full information about CCDC data access policies and citation 
# guidelines are available at http://www.ccdc.cam.ac.uk/access/V1 
# 
# Audit and citation data items may have been added by the CCDC. 
# Please retain this information to preserve the provenance of 
# this file and to allow appropriate attribution of the data. 
# 
#######################################################################

data_exp_13487
_audit_block_doi                 10.5517/ccdc.csd.cc2ghttm
_database_code_depnum_ccdc_archive 'CCDC 2279331'
loop_
_audit_author_name
_audit_author_address
lcr
;GXU
China
;
_audit_update_record             
;
2023-07-05 deposited with the CCDC.	2023-10-11 downloaded from the CCDC.
;
_audit_creation_date             2023-06-26
_audit_creation_method           
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_shelx_SHELXL_version_number     2014/7
_chemical_name_common            ?
_chemical_name_systematic        ?
_chemical_formula_moiety         'C24 H29 N3 O2 S'
_chemical_formula_sum            'C24 H29 N3 O2 S'
_chemical_formula_weight         423.56
_chemical_melting_point          ?
loop_
_atom_type_symbol
_atom_type_description
_atom_type_scat_dispersion_real
_atom_type_scat_dispersion_imag
_atom_type_scat_source
C C 0.0033 0.0016 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
H H 0.0000 0.0000 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
N N 0.0061 0.0033 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0106 0.0060 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
S S 0.1246 0.1234 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_shelx_space_group_comment       
;
The symmetry employed for this shelxl refinement is uniquely defined
by the following loop, which should always be used as a source of
symmetry information in preference to the above space-group names.
They are only intended as comments.
;
_space_group_crystal_system      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 1 21/n 1'
_space_group_name_Hall           '-P 2yn'
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x+1/2, y+1/2, -z+1/2'
'-x, -y, -z'
'x-1/2, -y-1/2, z-1/2'

_cell_length_a                   8.7303(9)
_cell_length_b                   18.2774(19)
_cell_length_c                   14.2998(14)
_cell_angle_alpha                90
_cell_angle_beta                 100.470(10)
_cell_angle_gamma                90
_cell_volume                     2243.8(4)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    2111
_cell_measurement_temperature    293
_cell_measurement_theta_max      24.2100
_cell_measurement_theta_min      4.0970
_shelx_estimated_absorpt_T_max   ?
_shelx_estimated_absorpt_T_min   ?
_exptl_absorpt_coefficient_mu    0.169
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.85711
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro 1.171.38.41 (Rigaku Oxford Diffraction, 2015)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_absorpt_special_details   ?
_exptl_crystal_colour            ?
_exptl_crystal_density_diffrn    1.254
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    ?
_exptl_crystal_description       block
_exptl_crystal_F_000             904
_exptl_crystal_size_max          0.2
_exptl_crystal_size_mid          0.15
_exptl_crystal_size_min          0.1
_exptl_transmission_factor_max   ?
_exptl_transmission_factor_min   ?
_diffrn_reflns_av_R_equivalents  0.0465
_diffrn_reflns_av_unetI/netI     0.0877
_diffrn_reflns_Laue_measured_fraction_full 0.997
_diffrn_reflns_Laue_measured_fraction_max 0.847
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_h_min       -10
_diffrn_reflns_limit_k_max       24
_diffrn_reflns_limit_k_min       -24
_diffrn_reflns_limit_l_max       17
_diffrn_reflns_limit_l_min       -19
_diffrn_reflns_number            10860
_diffrn_reflns_point_group_measured_fraction_full 0.997
_diffrn_reflns_point_group_measured_fraction_max 0.847
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         29.240
_diffrn_reflns_theta_min         3.384
_diffrn_ambient_temperature      293
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 8.0606
_diffrn_detector_type            Eos
_diffrn_measured_fraction_theta_full 0.997
_diffrn_measured_fraction_theta_max 0.847
_diffrn_measurement_details      
;
List of Runs (angles in degrees, time in seconds):

  # Type    Start    End  Width  tₑₓₚ   ω     θ     κ     φ   Frames
#--------------------------------------------------------------------------
  1  ω    -10.00  87.00   1.00    5.00    --   15.65  19.00 -60.00   97
  2  ω     55.00  83.00   1.00    5.00    --   15.65 178.00 150.00   28
  3  ω     44.00  86.00   1.00    5.00    --   15.65 178.00  60.00   42
  4  ω    -52.00   3.00   1.00    5.00    --   15.65 -38.00 150.00   55
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'Xcalibur, Eos, Gemini'
_diffrn_measurement_method       'ω scans'
_diffrn_orient_matrix_type       
'CrysAlisPro convention (1999,Acta A55,543-557)'
_diffrn_orient_matrix_UB_11      -0.0081883000
_diffrn_orient_matrix_UB_12      0.0260084000
_diffrn_orient_matrix_UB_13      -0.0374411000
_diffrn_orient_matrix_UB_21      0.0820532000
_diffrn_orient_matrix_UB_22      0.0011570000
_diffrn_orient_matrix_UB_23      0.0038129000
_diffrn_orient_matrix_UB_31      -0.0040588000
_diffrn_orient_matrix_UB_32      -0.0287928000
_diffrn_orient_matrix_UB_33      -0.0336188000
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'fine-focus sealed X-ray tube'
_diffrn_source_type              'Enhance (Mo) X-ray Source'
_reflns_Friedel_coverage         0.000
_reflns_Friedel_fraction_full    .
_reflns_Friedel_fraction_max     .
_reflns_number_gt                2965
_reflns_number_total             5155
_reflns_odcompleteness_completeness 99.62
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     26.32
_reflns_special_details          
;
 Reflections were merged by SHELXL according to the crystal
 class for the calculation of statistics and refinement.
 
 _reflns_Friedel_fraction is defined as the number of unique
 Friedel pairs measured divided by the number that would be
 possible theoretically, ignoring centric projections and
 systematic absences.
;
_reflns_threshold_expression     'I > 2σ(I)'
_computing_cell_refinement       'CrysAlisPro 1.171.38.41 (Rigaku OD, 2015)'
_computing_data_collection       'CrysAlisPro 1.171.38.41 (Rigaku OD, 2015)'
_computing_data_reduction        'CrysAlisPro 1.171.38.41 (Rigaku OD, 2015)'
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'XL (Sheldrick, 2008)'
_computing_structure_solution    'ShelXT (Sheldrick, 2015)'
_refine_diff_density_max         0.262
_refine_diff_density_min         -0.257
_refine_diff_density_rms         0.055
_refine_ls_extinction_coef       .
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.055
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     275
_refine_ls_number_reflns         5155
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.1409
_refine_ls_R_factor_gt           0.0768
_refine_ls_restrained_S_all      1.055
_refine_ls_shift/su_max          0.001
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'w=1/[σ²(Fo²)+(0.0552P)²+0.3318P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1385
_refine_ls_wR_factor_ref         0.1671
_refine_special_details          ?
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2.a Secondary CH2 refined with riding coordinates:
 C11(H11A,H11B), C12(H12A,H12B), C10(H10A,H10B), C13(H13A,H13B)
2.b Aromatic/amide H refined with riding coordinates:
 C5(H5), C8(H8), C24(H24), C20(H20), C7(H7), C6(H6), C21(H21), C22(H22),
 C23(H23)
2.c Idealised Me refined as rotating group:
 C1(H1A,H1B,H1C), C16(H16A,H16B,H16C), C17(H17A,H17B,H17C), C15(H15A,H15B,H15C)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     dual
_atom_sites_solution_secondary   ?
loop_
_atom_site_label
_atom_site_type_symbol
_atom_site_fract_x
_atom_site_fract_y
_atom_site_fract_z
_atom_site_U_iso_or_equiv
_atom_site_adp_type
_atom_site_occupancy
_atom_site_site_symmetry_order
_atom_site_calc_flag
_atom_site_refinement_flags_posn
_atom_site_refinement_flags_adp
_atom_site_refinement_flags_occupancy
_atom_site_disorder_assembly
_atom_site_disorder_group
S1 S 1.05644(9) 0.29159(5) 0.61634(5) 0.0481(3) Uani 1 1 d . . . . .
O2 O 0.2091(2) 0.38803(11) 0.41368(13) 0.0481(5) Uani 1 1 d . . . . .
N1 N 0.8185(3) 0.38747(12) 0.79303(15) 0.0383(6) Uani 1 1 d . . . . .
N2 N 0.6867(3) 0.34479(12) 0.64287(16) 0.0364(6) Uani 1 1 d . . . . .
O1 O 0.2626(3) 0.26990(13) 0.38507(17) 0.0721(8) Uani 1 1 d . . . . .
N3 N 0.4187(3) 0.33484(13) 0.49936(17) 0.0445(6) Uani 1 1 d . . . . .
C2 C 0.8253(3) 0.35294(14) 0.70756(18) 0.0323(6) Uani 1 1 d . . . . .
C9 C 0.9657(3) 0.38748(14) 0.84822(18) 0.0360(7) Uani 1 1 d . . . . .
C3 C 0.9775(3) 0.33193(15) 0.70743(19) 0.0350(7) Uani 1 1 d . . . . .
C4 C 1.0670(3) 0.35338(15) 0.79704(19) 0.0362(7) Uani 1 1 d . . . . .
C19 C 1.0768(3) 0.19852(17) 0.6510(2) 0.0397(7) Uani 1 1 d . . . . .
C14 C 0.2924(3) 0.32588(17) 0.4296(2) 0.0413(7) Uani 1 1 d . . . . .
C5 C 1.2242(4) 0.34553(17) 0.8385(2) 0.0484(8) Uani 1 1 d . . . . .
H5 H 1.2935 0.3229 0.8055 0.058 Uiso 1 1 calc R . . . .
C18 C 0.0663(3) 0.39221(17) 0.3404(2) 0.0448(8) Uani 1 1 d . . . . .
C11 C 0.4403(4) 0.39775(16) 0.5637(2) 0.0489(8) Uani 1 1 d . . . . .
H11A H 0.3896 0.3885 0.6175 0.059 Uiso 1 1 calc R . . . .
H11B H 0.3930 0.4408 0.5306 0.059 Uiso 1 1 calc R . . . .
C12 C 0.6718(3) 0.28562(16) 0.5737(2) 0.0473(8) Uani 1 1 d . . . . .
H12A H 0.7233 0.2422 0.6030 0.057 Uiso 1 1 calc R . . . .
H12B H 0.7214 0.2995 0.5209 0.057 Uiso 1 1 calc R . . . .
C8 C 1.0166(4) 0.41420(16) 0.9401(2) 0.0491(8) Uani 1 1 d . . . . .
H8 H 0.9484 0.4370 0.9738 0.059 Uiso 1 1 calc R . . . .
C24 C 1.0211(4) 0.16981(17) 0.7278(2) 0.0488(8) Uani 1 1 d . . . . .
H24 H 0.9710 0.1999 0.7653 0.059 Uiso 1 1 calc R . . . .
C10 C 0.6116(3) 0.41137(16) 0.5984(2) 0.0455(8) Uani 1 1 d . . . . .
H10A H 0.6603 0.4257 0.5454 0.055 Uiso 1 1 calc R . . . .
H10B H 0.6249 0.4510 0.6443 0.055 Uiso 1 1 calc R . . . .
C20 C 1.1522(4) 0.1525(2) 0.5970(2) 0.0564(9) Uani 1 1 d . . . . .
H20 H 1.1912 0.1712 0.5456 0.068 Uiso 1 1 calc R . . . .
C7 C 1.1721(4) 0.40544(18) 0.9789(2) 0.0577(9) Uani 1 1 d . . . . .
H7 H 1.2092 0.4224 1.0401 0.069 Uiso 1 1 calc R . . . .
C6 C 1.2741(4) 0.37197(19) 0.9289(2) 0.0587(9) Uani 1 1 d . . . . .
H6 H 1.3784 0.3672 0.9569 0.070 Uiso 1 1 calc R . . . .
C13 C 0.5028(4) 0.26963(16) 0.5381(2) 0.0543(9) Uani 1 1 d . . . . .
H13A H 0.4934 0.2323 0.4892 0.065 Uiso 1 1 calc R . . . .
H13B H 0.4565 0.2508 0.5900 0.065 Uiso 1 1 calc R . . . .
C1 C 0.6778(4) 0.40120(18) 0.8303(2) 0.0546(9) Uani 1 1 d . . . . .
H1A H 0.6648 0.4530 0.8373 0.082 Uiso 1 1 calc GR . . . .
H1B H 0.6853 0.3779 0.8911 0.082 Uiso 1 1 calc GR . . . .
H1C H 0.5899 0.3819 0.7871 0.082 Uiso 1 1 calc GR . . . .
C21 C 1.1696(4) 0.0796(2) 0.6186(3) 0.0743(12) Uani 1 1 d . . . . .
H21 H 1.2198 0.0493 0.5815 0.089 Uiso 1 1 calc R . . . .
C22 C 1.1140(4) 0.0509(2) 0.6941(3) 0.0720(11) Uani 1 1 d . . . . .
H22 H 1.1260 0.0013 0.7082 0.086 Uiso 1 1 calc R . . . .
C23 C 1.0402(4) 0.09576(19) 0.7489(3) 0.0634(10) Uani 1 1 d . . . . .
H23 H 1.0028 0.0764 0.8005 0.076 Uiso 1 1 calc R . . . .
C16 C -0.0479(4) 0.3344(2) 0.3520(3) 0.0869(14) Uani 1 1 d . . . . .
H16A H -0.0081 0.2876 0.3373 0.130 Uiso 1 1 calc GR . . . .
H16B H -0.1445 0.3438 0.3097 0.130 Uiso 1 1 calc GR . . . .
H16C H -0.0649 0.3342 0.4164 0.130 Uiso 1 1 calc GR . . . .
C17 C 0.0024(5) 0.4666(2) 0.3594(4) 0.1078(17) Uani 1 1 d . . . . .
H17A H -0.0263 0.4668 0.4211 0.162 Uiso 1 1 calc GR . . . .
H17B H -0.0876 0.4771 0.3119 0.162 Uiso 1 1 calc GR . . . .
H17C H 0.0805 0.5032 0.3572 0.162 Uiso 1 1 calc GR . . . .
C15 C 0.1108(5) 0.3913(3) 0.2442(2) 0.116(2) Uani 1 1 d . . . . .
H15A H 0.1925 0.4262 0.2426 0.174 Uiso 1 1 calc GR . . . .
H15B H 0.0219 0.4040 0.1969 0.174 Uiso 1 1 calc GR . . . .
H15C H 0.1464 0.3433 0.2313 0.174 Uiso 1 1 calc GR . . . .


_geom_special_details            
;
 All esds (except the esd in the dihedral angle between two l.s. planes)
 are estimated using the full covariance matrix.  The cell esds are taken
 into account individually in the estimation of esds in distances, angles
 and torsion angles; correlations between esds in cell parameters are only
 used when they are defined by crystal symmetry.  An approximate (isotropic)
 treatment of cell esds is used for estimating esds involving l.s. planes.
;
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
_geom_bond_site_symmetry_2
_geom_bond_publ_flag
S1 C3 1.744(3) . ?
S1 C19 1.772(3) . ?
O2 C14 1.346(3) . ?
O2 C18 1.477(3) . ?
N1 C2 1.386(3) . ?
N1 C9 1.380(3) . ?
N1 C1 1.447(3) . ?
N2 C2 1.391(3) . ?
N2 C12 1.455(3) . ?
N2 C10 1.471(3) . ?
O1 C14 1.208(3) . ?
N3 C14 1.356(3) . ?
N3 C11 1.463(3) . ?
N3 C13 1.456(4) . ?
C2 C3 1.384(4) . ?
C9 C4 1.394(4) . ?
C9 C8 1.396(4) . ?
C3 C4 1.429(4) . ?
C4 C5 1.399(4) . ?
C19 C24 1.384(4) . ?
C19 C20 1.387(4) . ?
C5 C6 1.375(4) . ?
C18 C16 1.482(4) . ?
C18 C17 1.513(5) . ?
C18 C15 1.497(4) . ?
C11 C10 1.508(4) . ?
C12 C13 1.499(4) . ?
C8 C7 1.379(4) . ?
C24 C23 1.390(4) . ?
C20 C21 1.369(5) . ?
C7 C6 1.382(5) . ?
C21 C22 1.366(5) . ?
C22 C23 1.373(5) . ?

loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
_geom_angle_site_symmetry_1
_geom_angle_site_symmetry_3
_geom_angle_publ_flag
C3 S1 C19 103.31(13) . . ?
C14 O2 C18 121.6(2) . . ?
C2 N1 C1 125.3(2) . . ?
C9 N1 C2 108.7(2) . . ?
C9 N1 C1 123.6(2) . . ?
C2 N2 C12 119.4(2) . . ?
C2 N2 C10 117.7(2) . . ?
C12 N2 C10 110.1(2) . . ?
C14 N3 C11 123.5(2) . . ?
C14 N3 C13 117.9(2) . . ?
C13 N3 C11 113.9(2) . . ?
N1 C2 N2 117.7(2) . . ?
C3 C2 N1 108.8(2) . . ?
C3 C2 N2 133.5(2) . . ?
N1 C9 C4 108.3(2) . . ?
N1 C9 C8 130.0(3) . . ?
C4 C9 C8 121.8(3) . . ?
C2 C3 S1 128.9(2) . . ?
C2 C3 C4 106.9(2) . . ?
C4 C3 S1 124.0(2) . . ?
C9 C4 C3 107.3(2) . . ?
C9 C4 C5 119.4(3) . . ?
C5 C4 C3 133.3(3) . . ?
C24 C19 S1 123.7(2) . . ?
C24 C19 C20 118.9(3) . . ?
C20 C19 S1 117.4(2) . . ?
O2 C14 N3 111.4(3) . . ?
O1 C14 O2 124.6(3) . . ?
O1 C14 N3 123.9(3) . . ?
C6 C5 C4 118.7(3) . . ?
O2 C18 C16 112.4(3) . . ?
O2 C18 C17 102.2(2) . . ?
O2 C18 C15 109.0(3) . . ?
C16 C18 C17 110.1(3) . . ?
C16 C18 C15 112.8(3) . . ?
C15 C18 C17 109.9(4) . . ?
N3 C11 C10 110.1(2) . . ?
N2 C12 C13 109.7(2) . . ?
C7 C8 C9 117.4(3) . . ?
C19 C24 C23 119.7(3) . . ?
N2 C10 C11 110.1(2) . . ?
C21 C20 C19 120.6(3) . . ?
C8 C7 C6 121.5(3) . . ?
C5 C6 C7 121.2(3) . . ?
N3 C13 C12 111.5(2) . . ?
C22 C21 C20 120.8(4) . . ?
C21 C22 C23 119.5(4) . . ?
C22 C23 C24 120.6(3) . . ?

_olex2_submission_special_instructions 'No special instructions were received'
_oxdiff_exptl_absorpt_empirical_details 
;
Empirical correction (ABSPACK) includes:
- Absorption correction using spherical harmonics
- Frame scaling
;
_oxdiff_exptl_absorpt_empirical_full_max 1.257
_oxdiff_exptl_absorpt_empirical_full_min 0.783
