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HCID 67354024、化合物 → 5-Amino-2-hydroxy-N-methylbenzamide

HRID 522873
ノート
印刷プレビュー

反応式

HRID 522873 の反応式
C([O:8][C:9]1[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][C:10]=1[C:11]([NH:13][CH3:14])=[O:12])C1C=CC=CC=1>[Pd].CO>[NH2:19][C:16]1[CH:17]=[CH:18][C:9]([OH:8])=[C:10]([CH:15]=1)[C:11]([NH:13][CH3:14])=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 67354024HCID 67354024、化合物

生成物 1

HCID 198229045-Amino-2-hydroxy-N-methylbenzamide

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

To a flask charged with 2-(benzyloxy)-N-methyl-5-nitrobenzamide (176 mg, 1.061 mmol) was added MeOH (4 mL). The resulting suspension was thoroughly purged with nitrogen prior to the addition of 10% Pd/C (12 mg, 0.046 mmol). The reaction mixture was purged with H2 gas, and then stirred under at atmosphere of hydrogen overnight. The reaction mixture was filtered through Celite® (diatomaceous earth) and the filtrate dried under reduced pressure. The resulting 5-amino-2-hydroxy-N-methylbenzamide (90 mg, 99% crude yield) was used in next step without further purification.

後処理

  1. customThe resulting suspension was thoroughly purged with nitrogen
  2. customThe reaction mixture was purged with H2 gas
  3. filtrationThe reaction mixture was filtered through Celite® (diatomaceous earth)
  4. customthe filtrate dried under reduced pressure
  5. customThe resulting 5-amino-2-hydroxy-N-methylbenzamide (90 mg, 99% crude yield) was used in next step without further purification

出典と根拠

ORDレコード
ord-e7562d999bc24e8182f7d9f22f68fc9c
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09334269B2

反応ノート

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