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5-Chloro-2-fluorobenzene-1-carboximidamide → HCID 178517511, 화합물

HRID 1010860
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인쇄 미리보기

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HRID 1010860 반응식
[F:1][C:2]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([NH2:6])=[NH:5].C([O:14][C:15]([CH:17]1[C:21](=O)[CH2:20][CH2:19][O:18]1)=O)C>CCO>[Cl:11][C:8]1[CH:9]=[CH:10][C:2]([F:1])=[C:3]([C:4]2[N:6]=[C:15]([OH:14])[C:17]3[O:18][CH2:19][CH2:20][C:21]=3[N:5]=2)[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 219309795-Chloro-2-fluorobenzene-1-carboximidamideHCID 450902902-Furancarboxylicacid,tetrahydro-3-oxo-,ethylester(9CI)

생성물 1

HCID 178517511HCID 178517511, 화합물수율 53%

시약·촉매·용매 1

HCID 702Ethanol용매2회

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온도
80 °C

실험 절차

To a solution of 2-fluoro-5-chlorobenzamidine (1.05 g, 6.08 mmol, 1.2 eq) in EtOH (20 ml) was added 3-oxo-tetrahydrofuran-2-carboxylic acid ethyl ester (prepared according to Moyer, M. P; Feldman, P. L.; Rapoport, H. J. Org. Chem, 1985, 50, 5223-5230; 800 mg, 5.06 mmol, 1 eq) in ethanol (5 ml). The reaction mixture was heated to 80° C. overnight. The reaction mixture was cooled to r.t. and the crude residue was purified by flash column chromatography (5% MeOH in CHCl3) to afford a white solid 2-(5-chloro-2-fluorophenyl)-6,7-dihydrofuro[3,2-d]pyrimidin-4-ol (650 mg, 53%).

후처리

  1. temperatureThe reaction mixture was cooled to r.t.
  2. customthe crude residue was purified by flash column chromatography (5% MeOH in CHCl3)

출처 및 근거

ORD 기록
ord-4879a16d9fe746ce8dc6bfa2ec5d3f83
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977342B2

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