Isopropyl iodide → HCID 57378323, compound

HRID 70390Notes

Reaction equation

HRID 70390 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[SH:9].I[CH:11]([CH3:13])[CH3:12].[Cl:14][C:15]1[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][C:16]=1[C:25]([F:28])([F:27])[F:26]>>[Cl:14][C:15]1[CH:20]=[CH:19][C:18]([S:21]([NH:1][C:2]2[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=2[S:9][CH:11]([CH3:13])[CH3:12])(=[O:23])=[O:22])=[CH:17][C:16]=1[C:25]([F:28])([F:27])[F:26]

Participants

4

Reactant 3

HCID 6362Isopropyl iodideHCID 120002-Amino-4-chlorobenzenethiolHCID 27807194-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride

Product 1

HCID 57378323HCID 57378323, compound

Procedure

Following General Procedure A and B, the title compound was prepared from 2-amino-4-chloro-benzenethiol, 2-iodo-propane, and 4-chloro-3-(trifluoromethyl)benzene-1-sulfonyl chloride.

Sources & evidence

ORD record
ord-becc82daccdb4daaa48760ba7cd5f07c
Source dataset
uspto-grants-2014_09
Patent number
US08822530B2

Reaction notes

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