HCID 75005637、化合物 → HCID 90795739、化合物
反応式
[OH:1][CH:2]1[CH:8]2[NH:9][CH:5]([C:6]3[CH:13]=[CH:12][CH:11]=[CH:10][C:7]=32)[C:4]2[CH:14]=[CH:15][CH:16]=[CH:17][C:3]1=2>[Si]([O-])([O-])([O-])[O-].[Ag+].[Ag+].[Ag+].[Ag+].C1C=CC=CC=1>[NH:9]1[CH:8]2[C:2](=[O:1])[C:3]3[CH:17]=[CH:16][CH:15]=[CH:14][C:4]=3[CH:5]1[C:6]1[CH:13]=[CH:12][CH:11]=[CH:10][C:7]=12参加物
実験手順
A mixture of 1.5 g of 11-hydroxy-10,11-dihydro-5,10-imino-[5H]-dibenzo (a,d) cycloheptene dl cis, 60 ml of benzene and 3 g of silver silicate was refluxed with stirring for 45 minutes and then 1.5 g of silver silicate were added and reflux was continued for another hour. The mixture was filtered hot and the filter was washed with methylene chloride. The combined filtrates were washed with 2N hydrochloric acid and the acid phase was made alkaline with sodium hydroxide. The mixture was extracted with methylene chloride and the organic phase was dried over magnesium sulfate and distilled to dryness under reduced pressure. The residue was chromatographed over silica gel and eluted with a 95-5 mixture of chloroform-methanol to obtain 780 mg of 10,11-dihydro-5,10-imino-[5H]-dibenzo (a,d) cycloheptene-11-one dl melting at 100° C identical to that of Example 1.
後処理
- temperaturewas refluxed
- temperaturereflux
- waitwas continued for another hour
- filtrationThe mixture was filtered hot
- washthe filter was washed with methylene chloride
- washThe combined filtrates were washed with 2N hydrochloric acid
- extractionThe mixture was extracted with methylene chloride
- dry with materialthe organic phase was dried over magnesium sulfate
- distillationdistilled to dryness under reduced pressure
- customThe residue was chromatographed over silica gel
- washeluted with a 95-5 mixture of chloroform-methanol
出典と根拠
- ORDレコード
- ord-924d2451c8ec4d4386cd686cec77c691
- 出典データセット
- uspto-grants-1977_02
- 特許番号
- US04009273
反応ノート
読み込み中…