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Ethanol → HCID 178517509, 화합물

HRID 1354321
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인쇄 미리보기

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HRID 1354321 반응식
CO[C:3]([CH:5]1[CH2:9][CH2:8][CH2:7][C:6]1=[O:10])=O.[F:11][C:12]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:13]=1[C:14]([NH2:16])=[NH:15].[CH2:22](O)C>>[Cl:21][C:18]1[CH:19]=[CH:20][C:12]([F:11])=[C:13]([C:14]2[N:16]=[C:6]([OH:10])[C:5]3[CH2:3][CH2:22][CH2:7][CH2:8][C:9]=3[N:15]=2)[CH:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702Ethanol2회HCID 66328Cyclopentanecarboxylic acid, 2-oxo-, methyl esterHCID 219309795-Chloro-2-fluorobenzene-1-carboximidamide

생성물 1

HCID 178517509HCID 178517509, 화합물수율 78%

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온도
80 °C

실험 절차

To a solution of methyl-2-oxocyclopentane carboxylate (2 g, 11.8 mmol, 1 eq), in dry ethanol (20 ml) was added a solution of 2-fluoro-5-chlorobenzamidine (2.04 g, 11.8 mmol, 1 eq) in ethanol (20 ml) and the reaction mixture was heated to 80° C. overnight. The reaction mixture was cooled to rt and the solvent was removed in vacuo to afford a crude residue which was purified by recrystallization from hot ethyl acetate to afford 2-(5-chloro-2-fluorophenyl)-5,6,7,8-tetrahydroquinazolin-4-ol (2.56 g, 78%) as a white solid.

후처리

  1. temperatureThe reaction mixture was cooled to rt
  2. customthe solvent was removed in vacuo
  3. customto afford a crude residue which
  4. customwas purified by recrystallization from hot ethyl acetate

출처 및 근거

ORD 기록
ord-2f6e6288cf274211b6d11108ced88cbc
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07223766B2

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