반응식
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:12]3[C:20]4[C:15](=[CH:16][C:17]([O:21][CH3:22])=[CH:18][CH:19]=4)[C:14]([CH2:23][C:24]([OH:26])=[O:25])=[C:13]3[CH3:27])=[N:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1.S(Cl)(Cl)=O.CO.[C:34]([O-])(=O)C.[Na+]>C(O)C.C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:12]3[C:20]4[C:15](=[CH:16][C:17]([O:21][CH3:22])=[CH:18][CH:19]=4)[C:14]([CH2:23][C:24]([O:26][CH3:34])=[O:25])=[C:13]3[CH3:27])=[N:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1참가 물질
실험 절차
To a solution of anhydrous 1-(7-chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetic acid (1.0g.) in ethanol-free chloroform (30 ml; dried over calcium chloride) was added a solution of thionyl chloride (0.19 ml.) in chloroform (2ml). The resulting dark red solution was stirred at room temperature for 30 mins., and then methanol (20 ml.) was added. The mixture was heated under reflux for 30 mins., saturated sodium acetate solution (2 ml.) was added, and the mixture was concentrated in vacuo. Water (30 ml.) was added to the residue and the mixture was extracted with ether (3 × 30 ml.). The ether extracts were washed successively with saturated sodium hydrogen carbonate solution (30 ml.) and water (30 ml.), and dried (Na2SO4). Evaporation of the solvent gave a dark yellow oil, which slowly crystallised to give methyl 1-(7-chloroquinazolin-4-yl)-5-methoxy-2-methylindol-3-ylacetate, m.p. 112°-114° C.
후처리
- temperatureThe mixture was heated
- temperatureunder reflux for 30 mins
- concentrationthe mixture was concentrated in vacuo
- additionWater (30 ml.) was added to the residue
- extractionthe mixture was extracted with ether (3 × 30 ml.)
- washThe ether extracts were washed successively with saturated sodium hydrogen carbonate solution (30 ml.) and water (30 ml.)
- dry with materialdried (Na2SO4)
- customEvaporation of the solvent
- customgave a dark yellow oil, which
- customslowly crystallised
출처 및 근거
- ORD 기록
- ord-9fa89b6832194ee3a953211cb7b9b4c4
- 출처 데이터셋
- uspto-grants-1977_03
- 특허 번호
- US04012513
연결된 노트
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