HCID 75005637、化合物 → HCID 90795739、化合物

HRID 436605ノート

反応式

HRID 436605 の反応式
[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

4

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

  1. temperaturewas refluxed
  2. temperaturereflux
  3. waitwas continued for another hour
  4. filtrationThe mixture was filtered hot
  5. washthe filter was washed with methylene chloride
  6. washThe combined filtrates were washed with 2N hydrochloric acid
  7. extractionThe mixture was extracted with methylene chloride
  8. dry with materialthe organic phase was dried over magnesium sulfate
  9. distillationdistilled to dryness under reduced pressure
  10. customThe residue was chromatographed over silica gel
  11. 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

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