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Triethyl phosphonoacetate → 2-(4-Chlorophenyl)-5-trifluoromethylpyridazin-3-one

HRID 1700071
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반응식

HRID 1700071 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][N:9]=[CH:10][C:11](=O)[C:12]([F:15])([F:14])[F:13])=[CH:4][CH:3]=1.[CH2:17]([O:19]P(CC(OCC)=O)(OCC)=O)[CH3:18]>C(N(CC)CC)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:17](=[O:19])[CH:18]=[C:11]([C:12]([F:15])([F:14])[F:13])[CH:10]=[N:9]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 13345Triethyl phosphonoacetateHCID 691428133,3,3-Trifluoro-2-oxopropanal 1-(4-chlorophenylhydrazone)

생성물 1

HCID 110548972-(4-Chlorophenyl)-5-trifluoromethylpyridazin-3-one수율 52.9%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

First, 2 g of 3,3,3-trifluoro-2-oxo-1-propanal 1-(4-chlorophenylhydrazone) and 2 g of ethyl diethylphosphonoacetate were mixed with 20 ml of triethylamine, and the reaction was allowed to proceed at 50° C. for 24 hours. The solvent was distilled out under reduced pressure, and the residue was subjected to column chromatography, which afforded 1.16 g of 2-(4-chlorophenyl)-5-trifluoromethylpyridazin-3-one (compound 1-332).

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후처리

  1. distillationThe solvent was distilled out under reduced pressure

출처 및 근거

ORD 기록
ord-c93e6cfd88b04220aaaffe199573f141
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06348628B1

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