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[Cl:1][C:2]1[CH:3]=[N:4][C:5](O)=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].CN(C)C=O.S(O[CH2:23][CH3:24])(OCC)=O.S(Cl)([Cl:27])=O>>[Cl:27][C:5]1[N:4]=[CH:3][C:2]([Cl:1])=[CH:10][C:6]=1[C:7]([O:9][CH2:23][CH3:24])=[O:8]참가 물질
실험 절차
5-Chloro-2-hydroxynicotinic acid [11.95 g; Synthetic Comm. (1989), 19, 553] was suspended in thionyl chloride (52 mL) and anhydrous dimethylformamide (2 mL) was added. The suspension was refluxed 3 h, then concentrated under a nitrogen stream to remove the bulk of excess thionyl chloride before adding anhydrous ethanol (30 mL) giving a mixture of the desired ester and diethyl sulfite. The resulting mixture was concentrated in vacuo to remove the ethanol yielding a suspension. The solids were then filtered off and washed with anhydrous diethyl ether (2×10 mL). The combined filtrates were concentrated in vacuo yielding crude product. Purification by silica gel chromatography (ethyl acetate:hexanes 8:92) gave pure title compound (4.75 g).
후처리
- temperatureThe suspension was refluxed 3 h
- concentrationconcentrated under a nitrogen
- customto remove the bulk of excess thionyl chloride
- additionbefore adding anhydrous ethanol (30 mL)
- customgiving
- concentrationThe resulting mixture was concentrated in vacuo
- customto remove the ethanol yielding a suspension
- filtrationThe solids were then filtered off
- washwashed with anhydrous diethyl ether (2×10 mL)
- concentrationThe combined filtrates were concentrated in vacuo
- customyielding crude product
- customPurification by silica gel chromatography (ethyl acetate:hexanes 8:92)
출처 및 근거
- ORD 기록
- ord-85c227ba86c94703860bb2d9efdc8202
- 출처 데이터셋
- uspto-grants-2007_07
- 특허 번호
- US07250518B2
연결된 노트
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