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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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methyl 3-(2-chloro-6-fluorophenyl)-2-hydrazinylidene-3-oxopropanoate → Methyl 5-chloro-4-oxo-1,4-dihydrocinnoline-3-carboxylate

HRID 598154
노트
인쇄 미리보기

반응식

HRID 598154 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4](F)[C:3]=1[C:9](=[O:17])[C:10](=[N:15][NH2:16])[C:11]([O:13][CH3:14])=[O:12]>COCCOCCOCCOC>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[C:9](=[O:17])[C:10]([C:11]([O:13][CH3:14])=[O:12])=[N:15][NH:16]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178501731methyl 3-(2-chloro-6-fluorophenyl)-2-hydrazinylidene-3-oxopropanoate

생성물 1

HCID 67267740Methyl 5-chloro-4-oxo-1,4-dihydrocinnoline-3-carboxylate수율 66.8%

시약·촉매·용매 1

HCID 8189Triglyme용매

반응 조건

온도
140 °C

실험 절차

A mixture of 4.2 g (16 mmol) of methyl 3-(2-chloro-6-fluorophenyl)-2-hydrazono-3-oxopropionate in 12 mL of triglyme was heated to 140° C. for 48 h. The slurry was then cooled to room temperature and the precipitate was collected by filtration. The precipitate was washed with diisopropyl ether and dried in vacuo to give 2.55 g (66%) of the title compound as a tan powder.

후처리

  1. temperatureThe slurry was then cooled to room temperature
  2. filtrationthe precipitate was collected by filtration
  3. washThe precipitate was washed with diisopropyl ether
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-a772b97b19494f9aba28cd908cd5b0b6
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07897607B2

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