반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[C@H:9]1[CH2:13][CH2:12][CH2:11][N:10]1[C:14]1[CH:19]=[CH:18][N:17]2[N:20]=[CH:21][C:22]([NH2:23])=[C:16]2[N:15]=1.Cl[C:25](=[O:30])[C:26](OC)=[O:27].C[CH2:32][N:33](C(C)C)[CH:34](C)C.CNC>C(Cl)Cl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[C@H:9]1[CH2:13][CH2:12][CH2:11][N:10]1[C:14]1[CH:19]=[CH:18][N:17]2[N:20]=[CH:21][C:22]([NH:23][C:25](=[O:30])[C:26]([N:33]([CH3:34])[CH3:32])=[O:27])=[C:16]2[N:15]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a DCM (1 mL) solution of (R)-5-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-amine (Preparation B; 50 mg, 0.16 mmol) was drop-wise added methyl 2-chloro-2-oxoacetate (19.4 mg, 0.159 mmol), followed by DIEA (0.0829 mL, 0.476 mmol). After the mild exothermal subsided and the reaction cooled back to ambient temperature, dimethylamine (0.8 mL, 1.6 mmol) [2M, THF] was added. The reaction was heated to gentle reflux for a few minutes, allowed to cool back to ambient temperature and stirred for 1 hour to reach completion. The reaction was concentrated and directly purified by reverse phase column chromatography, eluting with 5 to 60% acetonitrile/water to yield the final product as a pale-yellowish solid (48 mg, 73% yield). MS (apci) m/z=415.1 (M+H).
후처리
- temperatureThe reaction was heated
- temperatureto gentle reflux for a few minutes
- temperatureto cool back to ambient temperature
- concentrationThe reaction was concentrated
- customdirectly purified by reverse phase column chromatography
- washeluting with 5 to 60% acetonitrile/water
출처 및 근거
- ORD 기록
- ord-d42e2109b1a94fb8a69fff61596accce
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09447104B2
연결된 노트
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