Oxirane, [(2,3-dimethylphenoxy)methyl]- → HCID 13506768, 화합물
반응식
[CH3:1][O:2][C:3]([C:5]1[CH:14]([C:15]2[C:20]([F:21])=[CH:19][CH:18]=[C:17]([Cl:22])[C:16]=2[Cl:23])[C:13]2[C:12](=[O:24])[CH2:11][NH:10][CH2:9][C:8]=2[NH:7][C:6]=1[CH3:25])=[O:4].[CH3:26][C:27]1[C:37]([CH3:38])=[CH:36][CH:35]=[CH:34][C:28]=1[O:29][CH2:30][CH:31]1[O:33][CH2:32]1>CO.Cl>[CH3:1][O:2][C:3]([C:5]1[CH:14]([C:15]2[C:20]([F:21])=[CH:19][CH:18]=[C:17]([Cl:22])[C:16]=2[Cl:23])[C:13]2[C:12](=[O:24])[CH2:11][N:10]([CH2:32][CH:31]([OH:33])[CH2:30][O:29][C:28]3[CH:34]=[CH:35][CH:36]=[C:37]([CH3:38])[C:27]=3[CH3:26])[CH2:9][C:8]=2[NH:7][C:6]=1[CH3:25])=[O:4]참가 물질
실험 절차
4-(2,3-Dichloro-6-fluorophenyl)-1,4,5,6,7,8-hexahydro-2-methyl-5-oxo-1,7-naphthyridine-3-carboxylic acid methyl ester (12.1 g), 5.3 g of 3-(2,3-dimethylphenoxy)-1,2-epoxypropane and 150 ml of methanol were combined and refluxed for 18 hours. The alcohol was evaporated in vacuo. The residue was chromatographed on silica-gel using a 5% methanol-ethyl acetate system. The residue obtained on evaporation was dissolved in methanol and saturated with hydrogen chloride. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate. A precipitate formed on standing at room temperature. The solid was separated and treated with boiling acetonitrile. The solid was dried in vacuo to obtain 2.8 g of the title compound as the hydrochloride salt, m.p. 190°-3° C.
후처리
- temperaturerefluxed for 18 hours
- customThe alcohol was evaporated in vacuo
- customThe residue was chromatographed on silica-gel
- customThe residue obtained on evaporation
- customThe solvent was removed in vacuo
- dissolutionthe residue was dissolved in ethyl acetate
- customA precipitate formed
- customon standing at room temperature
- customThe solid was separated
- additiontreated with boiling acetonitrile
- customThe solid was dried in vacuo
출처 및 근거
- ORD 기록
- ord-4355266d43dd4e3a86a1977d7e5b7d1f
- 출처 데이터셋
- uspto-grants-1985_11
- 특허 번호
- US04551534
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