Potassium Carbonate → 2-chloro-7-cyclopentyl-5-methyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid methyl ester
반응식
Br[C:2]1[C:3]([NH:9][CH:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[Cl-].[Li+].C(=O)([O-])[O-].[K+].[K+].[CH3:23][O:24][C:25](=[O:29])[C:26]#[C:27][CH3:28]>CN(C=O)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:23][O:24][C:25]([C:26]1[N:9]([CH:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)[C:3]2[N:4]=[C:5]([Cl:8])[N:6]=[CH:7][C:2]=2[C:27]=1[CH3:28])=[O:29]참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 120 °C
실험 절차
A solution of (5-Bromo-2-chloro-pyrimidin-4-yl)cyclopentylamine (8 g, 28.93 mmol), lithium chloride (1.23 g, 28.9 mmol), potassium carbonate (10 g, 72 mmol) and palladium acetate (324.68 mg, 1.45 mmol) in DMF (300 mL) is degassed and back-filled filled with nitrogen three times. Methyl-2-butynoate (8.5 mL, 87 mmol) is added and the reaction solution is heated at 120° C. for 5 h. LC-MS indicated the formation of two regioisomers and no starting material remaining. After cooling to room temperature the solution is filtered through Celite, diluted with water and extracted with ethyl acetate three times. The organic layers are combined, washed with brine and dried over anhydrous sodium sulfate. The solvent is evaporated and the crude product is purified using silica gel chromatography (˜20% ethyl acetate/80% hexane) to give 2-chloro-7-cyclopentyl-5-methyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid methyl ester as a yellow solid (2.11 g, 25%). [M+H]+=294.04.
후처리
- additionback-filled
- additionfilled with nitrogen three times
- temperatureAfter cooling to room temperature the solution
- filtrationis filtered through Celite
- additiondiluted with water
- extractionextracted with ethyl acetate three times
- washwashed with brine
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent is evaporated
- customthe crude product is purified
출처 및 근거
- ORD 기록
- ord-a4a11c94133249618454438801db53cc
- 출처 데이터셋
- uspto-grants-2012_12
- 특허 번호
- US08324225B2
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