3-Amino-4-fluorophenol → 2-(4-bromobenzyl)-N-(2-fluoro-5-hydroxyphenyl)-3-oxobutyramide

HRID 1922142Notes

Reaction equation

HRID 1922142 reaction equation
C(S[C:6](=[O:19])[CH:7]([CH2:11][C:12]1[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][CH:13]=1)[C:8](=[O:10])[CH3:9])(C)(C)C.[NH2:20][C:21]1[CH:22]=[C:23]([OH:28])[CH:24]=[CH:25][C:26]=1[F:27]>>[Br:18][C:15]1[CH:14]=[CH:13][C:12]([CH2:11][CH:7]([C:8](=[O:10])[CH3:9])[C:6]([NH:20][C:21]2[CH:22]=[C:23]([OH:28])[CH:24]=[CH:25][C:26]=2[F:27])=[O:19])=[CH:17][CH:16]=1

Participants

3

Procedure

The title compound was prepared by the method of Preparation 11b using 2-(4-bromobenzyl)-3-oxothiobutyric acid S-tert-butyl ester and 3-amino-4-fluoro-phenol.

Sources & evidence

ORD record
ord-e9f334a912aa4c3ab883250ea10abfc9
Source dataset
uspto-grants-2012_05
Patent number
US08173812B2

Reaction notes

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