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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-(3-chlorophenyl)-4,5-dihydro-1H-pyrazol-3-amine → 1-(3-chlorophenyl)-1H-pyrazol-3-amine

HRID 26276
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HRID 26276 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[CH2:12][CH2:11][C:10]([NH2:13])=[N:9]2)[CH:5]=[CH:6][CH:7]=1>C(O)C.Cl[Cu]>[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[CH:12]=[CH:11][C:10]([NH2:13])=[N:9]2)[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 155806681-(3-chlorophenyl)-4,5-dihydro-1H-pyrazol-3-amine

생성물 1

HCID 136269421-(3-chlorophenyl)-1H-pyrazol-3-amine수율 72.9%

시약·촉매·용매 2

HCID 62652Cuprous chloride촉매HCID 702Ethanol용매

실험 절차

In the same apparatus and following the same modalities as in Example 1, 5 g (0.0255 mole) of 1-(m-chlorophenyl)-3-amino-2-pyrazoline were suspended in 25 ml of ethanol with addition of 0.2 g of CuCl, under an oxygen head. Oxidation was concluded after about 3 hours. The oxidized product was recovered as in Example 1, obtaining 3.6 g of 1-(m-chlorophenyl)-3-aminopyrazole, melting at 106°-107° C.

후처리

  1. customThe oxidized product was recovered as in Example 1

출처 및 근거

ORD 기록
ord-55082323dc144dcb852e9283355811bf
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04149005

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