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[H-].[Na+].[OH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1.[CH2:10]([O:12][C:13](=[O:22])[CH:14](Br)[C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)[CH3:11]>CN(C=O)C>[CH2:10]([O:12][C:13](=[O:22])[CH:14]([C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)[O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)[CH3:11]참가 물질
실험 절차
Sodium hydride (520 mg; 21.8 mmol; 1.4 equiv) was stirred with 2-hydroxypyridine (1.73 g; 18.2 mmol; 1.2 equiv) in DMF (30 mL) for 15 min. This solution was added to an aliquot of bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 3.6 g; 15 mmol) in DMF (20 mL). After stirring overnight, at rt., the resulting opaque black solution was concentrated in vacuo, dissolved in 20% isopropyl alcohol/chloroform, washed 5 times with saturated NaHCO3(aq), washed twice with saturated NaCl(aq), and dried over Na2SO4(s). After filtration, the solution was concentrated in vacuo and purified by SiO2 column chromatography on two consecutive columns with a 1% methanol/chloroform mobile phase and then an ethyl acetate/hexanes mobile phase (30%, 40%, 50% step gradient). A light yellow oil (134 mg; approx. 3% yield) was isolated. MS(ES) calc'd: [M+H]+=259.2 m/z. Found: 259.1 m/z.
후처리
- concentration, the resulting opaque black solution was concentrated in vacuo
- dissolutiondissolved in 20% isopropyl alcohol/chloroform
- washwashed 5 times with saturated NaHCO3(aq)
- washwashed twice with saturated NaCl(aq)
- dry with materialdried over Na2SO4(s)
- filtrationAfter filtration
- concentrationthe solution was concentrated in vacuo
- custompurified by SiO2 column chromatography on two consecutive columns with a 1% methanol/chloroform mobile phase
- customA light yellow oil (134 mg; approx. 3% yield) was isolated
출처 및 근거
- ORD 기록
- ord-d94fa65d735a4eb0a54115991fc4408a
- 출처 데이터셋
- uspto-grants-2004_06
- 특허 번호
- US06743794B2
연결된 노트
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