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3-benzyloxy-N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-methyl-benzamide → N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-3-hydroxy-4-methyl-benzamide

HRID 1028424
ノート
印刷プレビュー

反応式

HRID 1028424 の反応式
C([O:8][C:9]1[CH:10]=[C:11]([CH:32]=[CH:33][C:34]=1[CH3:35])[C:12]([NH:14][C:15]1[CH:20]=[C:19]([C:21]([CH3:24])([CH3:23])[CH3:22])[CH:18]=[C:17]([NH:25][S:26]([CH3:29])(=[O:28])=[O:27])[C:16]=1[O:30][CH3:31])=[O:13])C1C=CC=CC=1.[H][H]>CO.O1CCCC1.[Pd]>[C:21]([C:19]1[CH:18]=[C:17]([NH:25][S:26]([CH3:29])(=[O:28])=[O:27])[C:16]([O:30][CH3:31])=[C:15]([NH:14][C:12](=[O:13])[C:11]2[CH:32]=[CH:33][C:34]([CH3:35])=[C:9]([OH:8])[CH:10]=2)[CH:20]=1)([CH3:24])([CH3:22])[CH3:23]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 672175483-benzyloxy-N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-methyl-benzamideHCID 178418361HCID 178418361、化合物

生成物 1

HCID 67217566N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-3-hydroxy-4-methyl-benzamide

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 887Methanol溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

7.10 g 3-benzyloxy-N-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenyl)-4-methyl-benzamide are hydrogenated in a mixture of 70 ml of methanol and 40 ml of tetrahydrofuran in the presence of 800 mg palladium on activated charcoal (10% Pd) at ambient temperature and 50 psi partial hydrogen pressure. Then the catalyst is suction filtered and the filtrate is evaporated down using the rotary evaporator. A white solid remains, which is reacted further without any further purification.

後処理

  1. filtrationfiltered
  2. customthe filtrate is evaporated down
  3. customthe rotary evaporator
  4. customA white solid remains, which is reacted further without any further purification

出典と根拠

ORDレコード
ord-15404f0639c14a02a2af7a618b06b3d4
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08735579B2

反応ノート

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