반응식
C(=O)([O-])[O-].[K+].[K+].[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]([NH:17][C:18]2[CH:19]=[N:20][CH:21]=[C:22]([C:24]([C:26]3[C:34]4[CH:33]=[N:32][CH:31]=[N:30][C:29]=4[NH:28][CH:27]=3)=[O:25])[CH:23]=2)=[O:16])=[CH:10][CH:9]=1.[CH3:35][S:36][CH2:37]Cl.O>CN(C=O)C>[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]([NH:17][C:18]2[CH:19]=[N:20][CH:21]=[C:22]([C:24]([C:26]3[C:34]4[CH:33]=[N:32][CH:31]=[N:30][C:29]=4[N:28]([CH2:35][S:36][CH3:37])[CH:27]=3)=[O:25])[CH:23]=2)=[O:16])=[CH:10][CH:9]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Potassium carbonate (38 mg, 0.275 mmol) was added to a stirring solution of 2-(4-chlorophenyl)-N-[5-(7H-pyrrolo[2,3-d]pyrimidin-5-ylcarbonyl)pyridin-3-yl]acetamide (Example 308, 60.0 mg, 0.153 mmol) in DMF (1.0 mL) at room temperature. After 10 min, chloromethyl methyl sulfide (19 μL, 0.23 mmol) was added to the mixture and the reaction was stirred for 24 hours at room temperature. Water (3 mL) was added to the mixture and it was extracted with EtOAc (3×5 mL). The combined organic fractions were washed with water (5 mL), brine (5 mL), dried over magnesium sulfate and concentrated under reduced pressure to give a pale yellow oil. The crude material was purified by column chromatography on silica gel (gradient of 100% DCM to 90:10:1 DCM/MeOH/NH3) to give the title compound as a pale yellow solid in 36% yield, 25 mg.
후처리
- extractionwas extracted with EtOAc (3×5 mL)
- washThe combined organic fractions were washed with water (5 mL), brine (5 mL)
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customto give a pale yellow oil
- customThe crude material was purified by column chromatography on silica gel (gradient of 100% DCM to 90:10:1 DCM/MeOH/NH3)
출처 및 근거
- ORD 기록
- ord-fca356c6ed5e4969beaf6def4f1f55c1
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08846698B2
연결된 노트
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