Ammonium Chloride → (7-(4-Amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)(4-methylpiperazin-1-yl)methanone
반응식
[F:1][C:2]1[CH:26]=[C:25]([N+:27]([O-])=O)[CH:24]=[CH:23][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][N:8]=[C:7]2[CH:11]=[C:12]([C:14]([N:16]3[CH2:21][CH2:20][N:19]([CH3:22])[CH2:18][CH2:17]3)=[O:15])[S:13][C:6]=12.[Cl-].[NH4+]>CO.O.[Zn]>[NH2:27][C:25]1[CH:24]=[CH:23][C:3]([O:4][C:5]2[CH:10]=[CH:9][N:8]=[C:7]3[CH:11]=[C:12]([C:14]([N:16]4[CH2:17][CH2:18][N:19]([CH3:22])[CH2:20][CH2:21]4)=[O:15])[S:13][C:6]=23)=[C:2]([F:1])[CH:26]=1참가 물질
6
반응물 2
생성물 1
시약·촉매·용매 3
실험 절차
Zinc (0.75 g, 11.53 mmol) was added to a suspension of 437 (1.2 g, 2.88 mmol) and ammonium chloride (0.31 g, 5.76 mmol) in a mixture of MeOH (30 mL) and water (5.10 mL). The suspension was heated to reflux for 50 min. After cooling to room temperature, the reaction mixture was filtered and concentrated. The residue was partitioned between DCM, water and ammonium hydroxide. The organic layer was collected, successively washed with water and brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by biotage (SNAP 50 g cartridge; MeOH/DCM: 0/100 to 20/80 over 30CV), to afford the title compound 438 (733 mg, 1.89 mmol, 66% yield) as a yellow solid. MS (m/z): 387.4 (M+H).
후처리
- temperatureThe suspension was heated
- temperatureto reflux for 50 min
- filtrationthe reaction mixture was filtered
- concentrationconcentrated
- customThe residue was partitioned between DCM, water and ammonium hydroxide
- customThe organic layer was collected
- washsuccessively washed with water and brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by biotage (SNAP 50 g cartridge; MeOH/DCM: 0/100 to 20/80 over 30CV)
출처 및 근거
- ORD 기록
- ord-7fcddb8e823c47d7a663f75284d4d132
- 출처 데이터셋
- uspto-grants-2014_12
- 특허 번호
- US08906852B2
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