反応式
[C:1]([C:3]1[CH:15]=[CH:14][C:6]2[O:7][C:8]([CH3:13])([CH3:12])[CH:9]3[O:11][CH:10]3[C:5]=2[CH:4]=1)#[N:2].[NH:16]1[CH2:21][CH2:20][CH2:19][CH2:18][C:17]1=[O:22].[H-].[Na+].O>CS(C)=O.C(OCC)(=O)C>[C:1]([C:3]1[CH:15]=[CH:14][C:6]2[O:7][C:8]([CH3:13])([CH3:12])[C@@H:9]([OH:11])[C@H:10]([N:16]3[CH2:21][CH2:20][CH2:19][CH2:18][C:17]3=[O:22])[C:5]=2[CH:4]=1)#[N:2]参加物
7
実験手順
6-Cyano-3,4-dihydro-2,2-dimethyl-3,4-epoxy-2H-benzo[b]pyran and 2-piperidone were stirred in dimethyl sulphoxide under nitrogen at room temperature. Sodium hydride (81% dispersion in mineral oil) was added during 5 mins. and the reaction stirred for a further 6 hours. Addition of water, extraction with ethyl acetate, drying of the organic phase with magnesium sulpate, filtration, evaporation and recrystallisation from ethyl acetate gave 6-cyano-3,4-dihydro-2,2-dimethyl-trans-4-(2-oxo-1-piperidinyl)-2H-benzo[b]pyran-3-ol was prepared, as crystals of m.p. 155° C.
後処理
- dry with materialdrying of the organic phase with magnesium sulpate, filtration, evaporation and recrystallisation from ethyl acetate
出典と根拠
- ORDレコード
- ord-2623fdde1a7947069d7976ff1131d293
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04610992
関連ノート
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