Dimethylformamide dimethyl acetal → 1,5-dimethyl-1,6-naphthyridin-2(1H)-one
反応式
[CH3:1][C:2]1[N:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](=[O:12])[NH:7]2.[CH3:13]OC(OC)N(C)C>CN(C)C=O>[CH3:13][N:7]1[C:8]2[C:3](=[C:2]([CH3:1])[N:11]=[CH:10][CH:9]=2)[CH:4]=[CH:5][C:6]1=[O:12]参加物
4
実験手順
A mixture containing 4.5 g of 5-methyl-1,6-naphthyridin-2(1H)-one, 15 ml of dimethylformamide and 4 ml of dimethylformamide dimethyl acetal was stirred at room temperature overnight, then heated on a steam bath for 7 hours and then evaporated to dryness on a rotary evaporator. The solid residue was recrystallized from isopropyl alcohol and dried at 90°-95° C. to yield 3.5 g of 1,5-dimethyl-1,6-naphthyridin-2(1H)-one, m.p. 203°-205° C.
後処理
- temperatureheated on a steam bath for 7 hours
- customevaporated to dryness on a rotary evaporator
- customThe solid residue was recrystallized from isopropyl alcohol
- customdried at 90°-95° C.
出典と根拠
- ORDレコード
- ord-6c27ef1239c546e7856e5d12b96a5df6
- 出典データセット
- uspto-grants-1985_12
- 特許番号
- US04559347
反応ノート
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