2-Aminophenol → 4-Fluoro-N-(2-hydroxyphenyl)benzamide

HRID 59634ノート

反応式

HRID 59634 の反応式
FC1C=CC(C(Cl)=O)=CC=1.NC1C=CC=CC=1O.[F:19][C:20]1[CH:44]=[CH:43][C:23]([C:24]([NH:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[O:33]C(=O)C2C=CC(F)=CC=2)=[O:25])=[CH:22][CH:21]=1>>[F:19][C:20]1[CH:44]=[CH:43][C:23]([C:24]([NH:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[OH:33])=[O:25])=[CH:22][CH:21]=1

参加物

4

反応物 3

HCID 58012-AminophenolHCID 678794-Fluorobenzoyl chloride3 回HCID 1177721904-fluoro-Benzoic acid 2-[(4-fluorobenzoyl)amino]phenyl ester

生成物 1

HCID 5793834-Fluoro-N-(2-hydroxyphenyl)benzamide

実験手順

The examples below serve to illustrate the process according to the invention in more detail. 4-fluorobenzoic chloride (B) was added drop wise to a mixture of 2-aminophenol (A) in the respective solvent. The concentration of the 4-fluorobenzoic chloride (B) in the solvent [g/ml] is given in table 1. Afterwards the reaction was stirred under nitrogen. The conditions and results are listed in table 1. The amount of base is given as mol-equivalents based on the amount of 4-fluorobenzoic chloride (B). The reaction mixtures were analyzed after the indicated time by HPLC (254 nm, area %) in particular for determining the amount of 4-fluoro-Benzoic acid 2-[(4-fluorobenzoyl)amino]phenyl ester (i.e. the diacylated product, DAP). Then, 4-Fluoro-N-(2-hydroxyphenyl)-benzamide (IVa) was isolated resulting in the yields as indicated in the table 1 (purity >98% (HPLC at 254 nm)).

後処理

  1. customThe conditions and results
  2. customThe reaction mixtures

出典と根拠

ORDレコード
ord-a26cc490863d4dafa88e7e36d02a3ada
出典データセット
uspto-grants-2016_09
特許番号
US09440935B2

反応ノート

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