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4-Fluoroaniline → 4-((4-Fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetate

HRID 712400
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HRID 712400 반응식
[C:1]([O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][C:14]=1[O:15][CH3:16])[N:11]=[CH:10][N:9]=[C:8]2Cl)(=[O:3])[CH3:2].[F:18][C:19]1[CH:25]=[CH:24][C:22]([NH2:23])=[CH:21][CH:20]=1>C(O)(C)C>[C:1]([O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][C:14]=1[O:15][CH3:16])[N:11]=[CH:10][N:9]=[C:8]2[NH:23][C:22]1[CH:24]=[CH:25][C:19]([F:18])=[CH:20][CH:21]=1)(=[O:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 97314-FluoroanilineHCID 220221604-Chloro-7-methoxyquinazolin-6-yl acetate

생성물 1

HCID 867294674-((4-Fluorophenyl)amino)-7-methoxyquinazolin-6-yl acetate수율 85.9%

시약·촉매·용매 1

HCID 3776Isopropanol용매

반응 조건

온도
83 °C

실험 절차

A suspension of 4-chloro-7-methoxyquinazolin-6-yl acetate (2.17 g), 4-fluoroaniline (1.00 mL) and isopropanol (40 mL) was stirred at 83° C. overnight. The reaction mixture was cooled to room temperature and filtered, the residue was washed with 100 mL of isopropanol and dried to afford the desired compound as a solid (2.42 g, 85.90%)

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationfiltered
  3. washthe residue was washed with 100 mL of isopropanol
  4. customdried

출처 및 근거

ORD 기록
ord-ddb5447f0fd543b196c90d44a20b99ef
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181277B2

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