反応式
CO[C:3](OC)(OC)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Cl:14][C:15]1[C:24]([NH:25][NH2:26])=[N:23][C:22]2[C:17](=[CH:18][CH:19]=[C:20]([Cl:27])[CH:21]=2)[N:16]=1>>[Cl:14][C:15]1[C:24]2[N:23]([C:3]([C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=3)=[N:26][N:25]=2)[C:22]2[C:17]([N:16]=1)=[CH:18][CH:19]=[C:20]([Cl:27])[CH:21]=2参加物
反応条件
- 温度
- 120 °C
実験手順
In a 250 ml. three-necked reaction flask equipped with mechanical stirrer and reflux condenser, there were placed 50.0 g. (0.274 mole) of trimethyl orthobenzoate that had been preheated to ca. 70° C. Stirring was commenced and 10.0 g (0.0437 mole) of 2,6-dichloro-3-hydrazinoquinoxaline, the product of Preparation L(a), were added thereto. The resulting reaction mixture was then heated at ca. 120° C., with continued stirring, for a period of 24 hours, followed by cooling to room temperature (~20° C.) and stirring overnight for approximately 16 hours to give a yellow slurry. The latter slurry was then filtered, and the recovered solid product was subsequently washed with two-50 ml. portions of ethanol and air-dried to constant weight to ultimately afford 9.8 g. (72%) of crude 4,8-dichloro-1-phenyl-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 305°-307° C. Mass Spectrum: m/e, 316/314 (P+).
後処理
- customthree-necked reaction flask equipped with mechanical stirrer
- temperaturereflux condenser
- customhad been preheated to ca. 70° C
- additionwere added
- customThe resulting reaction mixture
- temperatureby cooling to room temperature (~20° C.)
- stirringstirring overnight for approximately 16 hours
- customto give a yellow slurry
- filtrationThe latter slurry was then filtered
- washthe recovered solid product was subsequently washed with two-50 ml
- dry with materialportions of ethanol and air-dried to constant weight to ultimately afford 9.8 g
出典と根拠
- ORDレコード
- ord-d04dd74928e646e39719f3a0e9128a62
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04547501
関連ノート
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