Sodium Hydroxide → {1-[5-(1H-pyrazol-4-yl)-pyridin-2-yl]-cyclobutyl}-carbamic acid tert-butyl ester
반응식
[C:1]([O:5][C:6](=[O:19])[NH:7][C:8]1([C:12]2[CH:17]=[CH:16][C:15](I)=[CH:14][N:13]=2)[CH2:11][CH2:10][CH2:9]1)([CH3:4])([CH3:3])[CH3:2].C(OC([N:27]1[CH:31]=[C:30](B2OC(C)(C)C(C)(C)O2)[CH:29]=[N:28]1)=O)(C)(C)C.[O-]P([O-])([O-])=O.[K+].[K+].[K+].[OH-].[Na+]>COCCOC.O.CCO>[C:1]([O:5][C:6](=[O:19])[NH:7][C:8]1([C:12]2[CH:17]=[CH:16][C:15]([C:30]3[CH:31]=[N:27][NH:28][CH:29]=3)=[CH:14][N:13]=2)[CH2:11][CH2:10][CH2:9]1)([CH3:4])([CH3:3])[CH3:2]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 100 °C
실험 절차
To a mixture of [1-(5-iodo-pyridin-2-yl)-cyclobutyl]-carbamic acid tert-butyl ester (0.46 g, 1.23 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrazole-1-carboxylic acid tert-butyl ester (0.4 g, 1.35 mmol), and PdCl2(dppf)Cl2.dichloromethane complex (0.2 g, 0.25 mmol) in DME/H2O/EtOH (4 mL, 7:3:2) in a sealable microwave tube was added 1M K3PO4 (1.5 mL, 1.5 mmol). The tube was sealed and heated in microwave at 100° C. for 10 minutes and then 120° C. for 20 minutes. 2M NaOH was added (2 mL) and stirred for 10 minutes. The solution was extracted with EtOAc (100 mL). The organic phase was washed with brine, dried over MgSO4, filtered through diatomaceous earth, and concentrated. The crude oil was purified via normal phase flash chromatography on silica gel eluting with 0-6% MeOH/CH2Cl2, to afford {1-[5-(1H-pyrazol-4-yl)-pyridin-2-yl]-cyclobutyl}-carbamic acid tert-butyl ester (0.40 g) as a brown solid, m/z 315.5 [M+H]+.
후처리
- customThe tube was sealed
- extractionThe solution was extracted with EtOAc (100 mL)
- washThe organic phase was washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered through diatomaceous earth
- concentrationconcentrated
- customThe crude oil was purified via normal phase flash chromatography on silica gel eluting with 0-6% MeOH/CH2Cl2
출처 및 근거
- ORD 기록
- ord-aa4f67022714402f8362e0d108ff037c
- 출처 데이터셋
- uspto-grants-2013_11
- 특허 번호
- US08575360B2
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