Ammonia → 3-(4-(4-Fluorophenoxy)phenyl)propanimidamide
반응식
[F:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]#[N:16])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.C(Cl)(C)=O.[NH3:23]>C1(C)C=CC=CC=1.CO>[F:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15](=[NH:23])[NH2:16])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1참가 물질
실험 절차
To a solution of 3-(4-(4-fluorophenoxyl)phenyl)propanenitrile (4.4 g, 18.24 mmol) in toluene (25 mL) and methanol (5.94 mL) was added dropwise AcCl (6.48 mL, 91 mmol) at 0° C. in 5 min. The mixture was stirred at room temperature for 2 h. The mixture was cooled to 0° C. in an ice bath, and ammonia (26.1 mL, 182 mmol) in methanol was added dropwise in 5 min. The mixture was stirred at room temperature overnight. The mixture was filtered to remove the solid, and the solid was washed with toluene (40 mL) and methanol (40 mL). The combined filtrate was concentrated in vacuo, the residue was triturated with diethyl ether, the resulting white solid was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound (5.4 g, 16.12 mmol, 88% yield) as white solid. LCMS: rt=1.03 min, [M+H+]=259
후처리
- temperatureThe mixture was cooled to 0° C. in an ice bath
- stirringThe mixture was stirred at room temperature overnight
- filtrationThe mixture was filtered
- customto remove the solid
- washthe solid was washed with toluene (40 mL) and methanol (40 mL)
- concentrationThe combined filtrate was concentrated in vacuo
- customthe residue was triturated with diethyl ether
- filtrationthe resulting white solid was collected by filtration
- washwashed with diethyl ether
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-82a3282461eb4ef2beefb9caf4a49083
- 출처 데이터셋
- uspto-grants-2015_11
- 특허 번호
- US09174968B2
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