2-Chloro-3-(trifluoromethyl)phenol → HCID 86654779, compound

HRID 2363132Notes

Reaction equation

HRID 2363132 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:14]([NH:16][C:17]([C:19]2[N:20]=[C:21](Cl)[O:22][CH:23]=2)=[O:18])[CH3:15])[CH:5]=[C:6]([F:13])[C:7]=1[NH:8][S:9]([CH3:12])(=[O:11])=[O:10].[Cl:25][C:26]1[C:31]([C:32]([F:35])([F:34])[F:33])=[CH:30][CH:29]=[CH:28][C:27]=1[OH:36]>>[F:1][C:2]1[CH:3]=[C:4]([CH:14]([NH:16][C:17]([C:19]2[N:20]=[C:21]([O:36][C:27]3[CH:28]=[CH:29][CH:30]=[C:31]([C:32]([F:33])([F:34])[F:35])[C:26]=3[Cl:25])[O:22][CH:23]=2)=[O:18])[CH3:15])[CH:5]=[C:6]([F:13])[C:7]=1[NH:8][S:9]([CH3:12])(=[O:11])=[O:10]

Participants

3

Reactant 2

HCID 27366012-Chloro-3-(trifluoromethyl)phenolHCID 671108872-Chloro-oxazole-4-carboxylic acid [1-(3,5-difluoro-4-methanesulfonylamino-phenyl)-ethyl]-amide

Product 1

HCID 86654779HCID 86654779, compoundYield 74.1%

Procedure

2-Chloro-oxazole-4-carboxylic acid [1-(3,5-difluoro-4-methanesulfonylamino-phenyl)-ethyl]-amide (50 mg, 0.13 mmol) was reacted with 2-chloro-3-trifluoromethyl-phenol (53 mg, 0.26 mmol) to give the title compound (52 mg, 74%) after purification by column chromatography (gradient 12% to 100% EtOAc in n-hexane).

Sources & evidence

ORD record
ord-fd51362692cd454d98af3bc907aee0a4
Source dataset
uspto-grants-2014_04
Patent number
US08691855B2

Reaction notes

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