Dimethyl Sulfoxide → HCID 57248286, compound

HRID 2339323Notes

Reaction equation

[CH2:11]([CH3:12])[CH:13]1[C:14](=[O:81])[CH2:15][CH:16]([O:70][Si:71]([CH:72]([CH3:73])[CH3:74])([CH:75]([CH3:76])[CH3:77])[CH:78]([CH3:79])[CH3:80])[CH:17]([CH3:69])[CH:18]([C:52](=[CH:53][CH:54]2[CH2:55][CH:56]([O:61][c:62]3[cH:63][cH:64][cH:65][cH:66][cH:67]3)[CH:57]([OH:60])[CH2:58][CH2:59]2)[CH3:68])[O:19][C:20](=[O:51])[CH:21]2[CH2:22][CH2:23][CH2:24][CH2:25][N:26]2[C:27](=[O:50])[C:28](=[O:49])[C:29]2([OH:48])[CH:30]([CH3:47])[CH2:31][CH:32]([O:45][CH3:46])[CH:33]([CH:34]([O:42][CH3:43])[CH2:35][CH:36]([CH3:41])[CH2:37][C:38]([CH3:40])=[CH:39]1)[O:44]2.[CH2:89]([Cl:90])[Cl:91].[CH3:7][S:8](=[O:9])[CH3:10].[CH3:82][CH2:83][N:84]([CH2:85][CH3:86])[CH2:87][CH3:88].[Cl:1][C:2]([C:3]([Cl:4])=[O:5])=[O:6].[OH2:92]>>[CH2:11]([CH3:12])[CH:13]1[C:14](=[O:81])[CH2:15][CH:16]([O:70][Si:71]([CH:72]([CH3:73])[CH3:74])([CH:75]([CH3:76])[CH3:77])[CH:78]([CH3:79])[CH3:80])[CH:17]([CH3:69])[CH:18]([C:52](=[CH:53][CH:54]2[CH2:55][CH:56]([O:61][c:62]3[cH:63][cH:64][cH:65][cH:66][cH:67]3)[C:57](=[O:60])[CH2:58][CH2:59]2)[CH3:68])[O:19][C:20](=[O:51])[CH:21]2[CH2:22][CH2:23][CH2:24][CH2:25][N:26]2[C:27](=[O:50])[C:28](=[O:49])[C:29]2([OH:48])[CH:30]([CH3:47])[CH2:31][CH:32]([O:45][CH3:46])[CH:33]([CH:34]([O:42][CH3:43])[CH2:35][CH:36]([CH3:41])[CH2:37][C:38]([CH3:40])=[CH:39]1)[O:44]2

Participants

Reactant 6

HCID 679Dimethyl Sulfoxide

HCID 962Water

HCID 6344Dichloromethane

HCID 8471Triethylamine

HCID 65578Oxalyl chloride

HCID 57285756HCID 57285756, compound

Product 1

HCID 57248286HCID 57248286, compound

Sources & evidence

ORD record: ord-733c507adb21444ab06a96718ddfddc8
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D

Reaction notes

Loading…