Ethanesulfonyl chloride → HCID 23533364, compound

HRID 1218133Notes

Reaction equation

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

Participants

Reactant 2

HCID 11667Ethanesulfonyl chloride

HCID 9869645HCID 9869645, compound

Product 1

HCID 23533364HCID 23533364, compound

Sources & evidence

ORD record: ord-b6a3b5c6f3684f79a8c266509632df3e
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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