Dimethyl Sulfoxide → HCID 10231968, compound

HRID 186564Notes

Reaction equation

[CH3:42][S:43]([CH3:44])=[O:45].[OH:1][CH:2]([CH2:3][NH:4][CH:5]1[CH2:6][CH2:7][N:8]([c:11]2[cH:12][cH:13][c:14]([S:17](=[O:18])(=[O:19])[N:20]3[CH:21]([C:25](=[O:26])[O:27][CH2:28][CH3:29])[CH2:22][CH2:23][CH2:24]3)[cH:15][cH:16]2)[CH2:9][CH2:10]1)[c:30]1[cH:31][c:32]([NH:37][S:38](=[O:39])(=[O:40])[CH3:41])[c:33]([OH:36])[cH:34][cH:35]1>>[OH:1][CH:2]([CH2:3][NH:4][CH:5]1[CH2:6][CH2:7][N:8]([c:11]2[cH:12][cH:13][c:14]([S:17](=[O:18])(=[O:19])[N:20]3[CH:21]([C:25](=[O:26])[OH:27])[CH2:22][CH2:23][CH2:24]3)[cH:15][cH:16]2)[CH2:9][CH2:10]1)[c:30]1[cH:31][c:32]([NH:37][S:38](=[O:39])(=[O:40])[CH3:41])[c:33]([OH:36])[cH:34][cH:35]1

Participants

Reactant 2

HCID 679Dimethyl Sulfoxide

HCID 22713403HCID 22713403, compound

Product 1

HCID 10231968HCID 10231968, compound

Sources & evidence

ORD record: ord-ef739f5512f74c96b3c36a378e490066
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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