Sulfur → 3-Bromo-4-cyclopropyl-5-fluoropyridine
반응식
C1(OC([N:10]2[CH:15]=[C:14]([F:16])[CH:13]([CH:17]3[CH2:19][CH2:18]3)[C:12]([Br:20])=[CH:11]2)=O)C=CC=CC=1.[S]>C1C2C(CCCC2)CCC1>[Br:20][C:12]1[CH:11]=[N:10][CH:15]=[C:14]([F:16])[C:13]=1[CH:17]1[CH2:18][CH2:19]1참가 물질
4
실험 절차
A mixture of crude 3-bromo-4-cyclopropyl-5-fluoro-4H-pyridine-1-carboxylic acid phenyl ester (A; 7.5 g, 0.022 mol) and sulphur (0.71 g, 0.022 mol) were heated at reflux in DECALIN (25 mL) for a period of 3 h and then cooled to RT. The reaction mixture was purified by silica gel column chromatography, eluting first with hexane and then with a 2-5% ethyl acetate-hexane gradient to afford 3-bromo-4-cyclopropyl-5-fluoro-pyridine. 1H NMR (400 MHz, DMSO-d6) δ 8.54 (s, 1H), 8.42 (s, 1H), 1.98-1.94 (m, 1H), 1.11-1.09 (m, 2H), 0.99-0.98 (m, 2H). MS (M+1): 217.1.
후처리
- customThe reaction mixture was purified by silica gel column chromatography
- washeluting first with hexane
출처 및 근거
- ORD 기록
- ord-5ba2ee9dba564c71a4b1c909d838a790
- 출처 데이터셋
- uspto-grants-2015_11
- 특허 번호
- US09193724B2
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