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Dimethyl Sulfoxide → HCID 5275155, compound

HRID 320817
Notes
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Reaction equation

HRID 320817 reaction equation
[Br:17][CH2:18][C:19](=[O:20])[NH:21][c:22]1[c:23]([N+:28](=[O:29])[O-:30])[cH:24][cH:25][cH:26][cH:27]1.[CH3:37][S:38]([CH3:39])=[O:40].[OH2:41].[c:1]1(-[n:11]2[c:12](=[S:16])[nH:13][n:14][cH:15]2)[cH:2][cH:3][cH:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]12.[cH:31]1[cH:32][cH:33][n:34][cH:35][cH:36]1>>[c:1]1(-[n:11]2[c:12]([S:16][CH2:18][C:19](=[O:20])[NH:21][c:22]3[c:23]([N+:28](=[O:29])[O-:30])[cH:24][cH:25][cH:26][cH:27]3)[n:13][n:14][cH:15]2)[cH:2][cH:3][cH:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]12
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 962WaterHCID 1049PyridineHCID 2207872-Bromo-n-(2-nitrophenyl)acetamideHCID 28887991HCID 28887991, compound

Product 1

HCID 5275155HCID 5275155, compound

Sources & evidence

On this pageParticipantsSources & evidenceReaction notes
ORD record
ord-1472074a891744719fbb384bb1c70620
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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