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benzyl 4-[(methoxycarbonyl)amino]-1H-pyrrolo[3,2-c]pyridine-1-carboxylate → methyl 1H-pyrrolo[3,2-c]pyridin-4-ylcarbamate

HRID 875407
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반응식

HRID 875407 반응식
[CH3:1][O:2][C:3]([NH:5][C:6]1[C:11]2[CH:12]=[CH:13][N:14](C(OCC3C=CC=CC=3)=O)[C:10]=2[CH:9]=[CH:8][N:7]=1)=[O:4]>C(O)C.[Pd]>[NH:14]1[C:10]2[CH:9]=[CH:8][N:7]=[C:6]([NH:5][C:3](=[O:4])[O:2][CH3:1])[C:11]=2[CH:12]=[CH:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 71061748benzyl 4-[(methoxycarbonyl)amino]-1H-pyrrolo[3,2-c]pyridine-1-carboxylate

생성물 1

HCID 86720632methyl 1H-pyrrolo[3,2-c]pyridin-4-ylcarbamate수율 90.75%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a stirred solution of benzyl 4-[(methoxycarbonyl)amino]-1H-pyrrolo[3,2-c]pyridine-1-carboxylate (264 mg, 0.82 mmol, Step a) in ethanol (10 mL) was added catalytic amount of palladium on carbon (10% wet). The reaction mixture was stirred under an atmosphere of hydrogen gas (atmospheric pressure) for 1 hour. The reaction mixture was filtered over celite and the residue washed with ethanol. The filtrate was concentrated to yield methyl 1H-pyrrolo[3,2-c]pyridin-4-ylcarbamate as a white powder (141 mg, 90.75%).

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후처리

  1. filtrationThe reaction mixture was filtered over celite
  2. washthe residue washed with ethanol
  3. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-9bc0cea9212848dfb2a64ba502c2c9ce
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08980911B2

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