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Ethyl 4-chloro-3-ethyl-1-methyl-1H-pyrazole-5-carboxylate → HCID 14771162, 화합물

HRID 1073321
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인쇄 미리보기

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HRID 1073321 반응식
[Cl:1][C:2]1[C:3]([CH2:13][CH3:14])=[N:4][N:5]([CH3:12])[C:6]=1[C:7]([O:9]CC)=O.[NH2:15][CH2:16][C:17]1[CH:18]=[CH:19][C:20]([CH2:23][CH2:24][CH2:25][CH3:26])=[N:21][CH:22]=1>>[CH2:23]([C:20]1[N:21]=[CH:22][C:17]([CH2:16][NH:15][C:7]([C:6]2[N:5]([CH3:12])[N:4]=[C:3]([CH2:13][CH3:14])[C:2]=2[Cl:1])=[O:9])=[CH:18][CH:19]=1)[CH2:24][CH2:25][CH3:26]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14793330Ethyl 4-chloro-3-ethyl-1-methyl-1H-pyrazole-5-carboxylateHCID 14852810HCID 14852810, 화합물

생성물 1

HCID 14771162HCID 14771162, 화합물수율 61.4%

반응 조건

온도
200 °C

실험 절차

A mixture of 2.17 g of ethyl 4-chloro-3-ethyl-1-methylpyrazole-5-carboxylate and 3.24 g of 5-aminomethyl-2-n-butylpyridine was heated at 200° C. for 4 hours under stirring. After cooling to room temperature, the reaction mixture was purified by silica gel columnchromatography to obtain 2.06 g of the compound (NO. 15) listed in Table 1.

후처리

  1. temperatureAfter cooling to room temperature
  2. customthe reaction mixture was purified by silica gel columnchromatography

출처 및 근거

ORD 기록
ord-fe4859a313a049db9bda8204b53ca6ab
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04968805

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