Sodium Hydroxide → HCID 86732538、化合物

HRID 623305ノート

反応式

HRID 623305 の反応式
[Cl:1][C:2]1[C:3]([CH2:12][CH2:13][NH:14][C:15](=[O:26])[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[C:22]([F:25])([F:24])[F:23])=[N:4][CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.[OH-].[Na+]>CO>[Cl:1][C:2]1[C:3]([CH2:12][CH:13]=[N:14][C:15](=[O:26])[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[C:22]([F:23])([F:24])[F:25])=[N:4][CH:5]=[C:6]([C:8]([F:10])([F:9])[F:11])[CH:7]=1

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 11158353Fluopyram

生成物 1

HCID 86732538HCID 86732538、化合物収率 17.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

2.00 g of N-{2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]ethyl}-2-(trifluoromethyl)benzamide (Int-5), (known from WO 2004/016088), were dissolved in 20 mL of methanol. 1 mL of concentrated bleach was added to the reaction mixture at room temperature. The reaction mixture was stirred for 24 hours at room temperature. 20 mL of a 1N aqueous solution of sodium hydroxide were added to the reaction mixture which was then extracted twice with diethyl ether. The combined organic phases were dried over magnesium sulphate, concentrated in vacuo to yield 1.41 g of crude product which was purified by chromatography on silica gel with ethyl acetate/heptane (3/7 v/v) as eluting phase. 340 mg (17%) of desired N-{2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]ethylidene}-2-(trifluoromethyl)benzamide (Int-6) were obtained, [M+1]=395.

後処理

  1. addition1 mL of concentrated bleach was added to the reaction mixture at room temperature
  2. extractionwas then extracted twice with diethyl ether
  3. dry with materialThe combined organic phases were dried over magnesium sulphate
  4. concentrationconcentrated in vacuo
  5. customto yield 1.41 g of crude product which
  6. customwas purified by chromatography on silica gel with ethyl acetate/heptane (3/7 v/v)
  7. washas eluting phase

出典と根拠

ORDレコード
ord-124d1a98be6849aaa73782c8425bbb2c
出典データセット
uspto-grants-2016_04
特許番号
US09301526B2

反応ノート

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