반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][N:3]=1.C([Li])(C)(C)C.CCCCC.[Cl:19][C:20]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[N:23]=[C:22]([C:30](OCC)=[O:31])[N:21]=1.[Cl-].[NH4+]>C(OCC)C.C(OCC)C.C(Cl)Cl>[Cl:19][C:20]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[N:23]=[C:22]([C:30]([C:2]2[CH:7]=[CH:6][C:5]([F:8])=[CH:4][N:3]=2)=[O:31])[N:21]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- -78 °C
실험 절차
To a stirred solution of 2-bromo-5-fluoropyridine (237 mg, 2.11 mmol) in anhydrous diethyl ether (7 mL) at −78° C. was added dropwise 1.7 M tert-butyl lithium/pentane (4 mL, 6.8 mmol). The brown mixture was stirred at −78° C. for 20 min, then ethyl 4-chloroquinazoline-2-carboxylate (500 mg, 2.11 mmol) in 3:1 diethyl ether/DCM (4 mL) was added to the mixture over 40 min. The resulting mixture was stirred at −78° C. for 1 h and then at −40° C. for 4 h. Then 10% aq ammonium chloride was added and the mixture was extracted three times with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 0-50% EtOAc/hexane to afford (4-chloroquinazolin-2-yl)(5-fluoropyridin-2-yl)methanone (150 mg, 25%). 1H NMR (300 MHz, CDCl3) δ 8.50 (d, J=3 Hz, 1H), 8.37-8.28 (m, 2H), 8.17 (d, J=8.4 Hz, 1H), 8.04 (t, J=8.4 Hz, 1H), 7.83 (t, J=8.4 Hz, 1H), 7.63 (td, J=3 Hz, J=8.4 Hz, 1H); LC-MS (ESI) m/z 288 (M+H)+.
후처리
- stirringThe resulting mixture was stirred at −78° C. for 1 h
- waitat −40° C. for 4 h
- extractionthe mixture was extracted three times with EtOAc
- dry with materialThe combined organic layers were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel chromatography
- washeluting with 0-50% EtOAc/hexane
출처 및 근거
- ORD 기록
- ord-0007e011338f4cc6b6acbe402754d1a3
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08633207B2
연결된 노트
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