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N-(1-methyl-4-piperidyl)-7-nitro-benzo[1,3]dioxole-4-carboxamide → 7-amino-N-(1-methyl-4-piperidyl)benzo[1,3]dioxole-4-carboxamide

HRID 2234490
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인쇄 미리보기

반응식

HRID 2234490 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([NH:8][C:9]([C:11]2[C:19]3[O:18][CH2:17][O:16][C:15]=3[C:14]([N+:20]([O-])=O)=[CH:13][CH:12]=2)=[O:10])[CH2:4][CH2:3]1>CO>[NH2:20][C:14]1[C:15]2[O:16][CH2:17][O:18][C:19]=2[C:11]([C:9]([NH:8][CH:5]2[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]2)=[O:10])=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 68682205N-(1-methyl-4-piperidyl)-7-nitro-benzo[1,3]dioxole-4-carboxamide2회

생성물 1

HCID 686813937-amino-N-(1-methyl-4-piperidyl)benzo[1,3]dioxole-4-carboxamide수율 96%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

N-(1-methyl-4-piperidyl)-7-nitro-benzo[1,3]dioxole-4-carboxamide (Intermediate 224; 290 mg, 0.94 mmol) was suspended in methanol (50 mL) and the system purged with nitrogen. 10% Pd/C (30 mg) was added and the mixture stirred under a hydrogen atmosphere for 2 hours. The catalyst was filtered off and the filtrate evaporated to give the title compound as a white solid (249 mg, 96%).

후처리

custom
the system purged with nitrogen
  • addition10% Pd/C (30 mg) was added
  • filtrationThe catalyst was filtered off
  • customthe filtrate evaporated
  • 출처 및 근거

    ORD 기록
    ord-011a93a20bca4638b72e87552454e2e1
    출처 데이터셋
    uspto-grants-2010_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07709471B2

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