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HCID 67354024, 화합물 → 5-Amino-2-hydroxy-N-methylbenzamide

HRID 522873
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HRID 522873 반응식
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]
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참가 물질

4

반응물 1

HCID 67354024HCID 67354024, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-e7562d999bc24e8182f7d9f22f68fc9c
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09334269B2

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