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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3,3-Dimethyl-7-nitro-2,3-dihydro-isoindol-1-one → 3,3-Dimethyl-7-amino-2,3-dihydro-isoindol-1-one

HRID 2112107
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인쇄 미리보기

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HRID 2112107 반응식
[CH3:1][C:2]1([CH3:15])[C:10]2[C:5](=[C:6]([N+:11]([O-])=O)[CH:7]=[CH:8][CH:9]=2)[C:4](=[O:14])[NH:3]1>CO.[Pd]>[CH3:1][C:2]1([CH3:15])[C:10]2[C:5](=[C:6]([NH2:11])[CH:7]=[CH:8][CH:9]=2)[C:4](=[O:14])[NH:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 670953413,3-Dimethyl-7-nitro-2,3-dihydro-isoindol-1-one

생성물 1

HCID 670950073,3-Dimethyl-7-amino-2,3-dihydro-isoindol-1-one

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

67 mg (0.325 mmol) 3,3-dimethyl-7-nitro-2,3-dihydro-isoindol-1-one are dissolved in 50 ml of methanol and combined with 10 mg palladium on charcoal. The mixture is hydrogenated for 16 h at 4 bar H2 pressure and ambient temperature. Then the catalyst is filtered off and the solvent is eliminated in vacuo.

후처리

  1. filtrationThen the catalyst is filtered off

출처 및 근거

ORD 기록
ord-5abc06f3a19d4a38a44e89590cf20fc1
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07521457B2

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