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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-butyl-3-nitro-5-cyclopropyl-1H-pyrazole-1-carboxylate → tert-butyl 3-amino-5-cyclopropyl-1H-pyrazole-1-carboxylate

HRID 1935333
노트
인쇄 미리보기

반응식

HRID 1935333 반응식
[C:1]([O:5][C:6]([N:8]1[C:12]([CH:13]2[CH2:15][CH2:14]2)=[CH:11][C:10]([N+:16]([O-])=O)=[N:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(O)C.[Pd]>[C:1]([O:5][C:6]([N:8]1[C:12]([CH:13]2[CH2:14][CH2:15]2)=[CH:11][C:10]([NH2:16])=[N:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 11265267tert-butyl-3-nitro-5-cyclopropyl-1H-pyrazole-1-carboxylate

생성물 1

HCID 11218347tert-butyl 3-amino-5-cyclopropyl-1H-pyrazole-1-carboxylate수율 95%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

1.2 g (4.74 mmol) of tert-butyl-3-nitro-5-cyclopropyl-1H-pyrazole-1-carboxylate were dissolved in 20 ml of ethanol and hydrogenated in presence of 200 mg of palladium on charcoal 10% at 50 psi and room temperature to give, after filtration on celite and evaporation of the solvent, 0.96 g (95% yield) of the title compound.

후처리

  1. customto give
  2. filtrationafter filtration

출처 및 근거

ORD 기록
ord-f5fa94ed91264816b207650519461718
출처 데이터셋
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06387900B1

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