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4-Chloro-3-(pyridin-2-yl)aniline → HCID 58614721, compound

HRID 202165
Notes
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Reaction equation

HRID 202165 reaction equation
[CH3:15][S:16](=[O:17])(=[O:18])[c:19]1[n:20][cH:21][c:22]([C:23](=[O:24])[OH:25])[cH:26][cH:27]1.[Cl:1][c:2]1[c:3](-[c:9]2[n:10][cH:11][cH:12][cH:13][cH:14]2)[cH:4][c:5]([NH2:6])[cH:7][cH:8]1>>[Cl:1][c:2]1[c:3](-[c:9]2[n:10][cH:11][cH:12][cH:13][cH:14]2)[cH:4][c:5]([NH:6][C:23]([c:22]2[cH:21][n:20][c:19]([S:16]([CH3:15])(=[O:17])=[O:18])[cH:27][cH:26]2)=[O:24])[cH:7][cH:8]1
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 401519254-Chloro-3-(pyridin-2-yl)anilineHCID 534296166-(Methylsulfonyl)nicotinic Acid

Product 1

HCID 58614721HCID 58614721, compound

Sources & evidence

ORD record
ord-b725075a358d4b35880bcde422829b1e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes