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2-Amino-4-chlorobenzenethiol → N-{5-chloro-2-[(pyridin-3-ylmethyl)thio]phenyl}-1-benzofuran-2-sulfonamide

HRID 2097751
Notes
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Reaction equation

HRID 2097751 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[SH:9].Br.Br[CH2:12][C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1.[O:19]1[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=2[CH:21]=[C:20]1[S:28](Cl)(=[O:30])=[O:29]>>[Cl:8][C:6]1[CH:5]=[CH:4][C:3]([S:9][CH2:12][C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)=[C:2]([NH:1][S:28]([C:20]2[O:19][C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=3[CH:21]=2)(=[O:29])=[O:30])[CH:7]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 120002-Amino-4-chlorobenzenethiolHCID 27951721-Benzofuran-2-sulfonyl chlorideHCID 127070373-(Bromomethyl)pyridine hydrobromide

Product 1

HCID 57377780N-{5-chloro-2-[(pyridin-3-ylmethyl)thio]phenyl}-1-benzofuran-2-sulfonamide

Procedure

Following General Procedure A and B, the title compound was prepared from 2-amino-4-chloro-benzenethiol, 3-bromomethyl-pyridine hydrobromide, and benzofuran-2-sulfonyl chloride.

Sources & evidence

ORD record
ord-b7a5ac9b0a05406ea4d41b92bfed6ca5
Source dataset
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08450367B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes