Hydrochloric Acid → 1-(2-isopropylaminopropyl)-9-methoxy-3-methyl-3,4,5,5a,6,7-hexahydro-2H-naphth[1,2-d]azepin-2-one

HRID 46515ノート

反応式

HRID 46515 の反応式
O=[C:2]([CH3:23])[CH2:3][C:4]1[C:5](=[O:22])[N:6]([CH3:21])[CH2:7][CH2:8][CH:9]2[CH2:18][CH2:17][C:16]3[C:11](=[CH:12][CH:13]=[C:14]([O:19][CH3:20])[CH:15]=3)[C:10]=12.[CH:24]([NH2:27])([CH3:26])[CH3:25].Cl.C([BH3-])#N.[Na+]>CO>[CH:24]([NH:27][CH:2]([CH3:23])[CH2:3][C:4]1[C:5](=[O:22])[N:6]([CH3:21])[CH2:7][CH2:8][CH:9]2[CH2:18][CH2:17][C:16]3[C:11](=[CH:12][CH:13]=[C:14]([O:19][CH3:20])[CH:15]=3)[C:10]=12)([CH3:26])[CH3:25]

参加物

6

実験手順

The mixture of 4.7 g of 1-(2-oxopropyl)-9-methoxy-3-methyl-3,4,5,5a,6,7-hexahydro-2H-naphth[1,2-d]azepin-2-one, 8.88 ml of isopropylamine, 3.45 ml of 5 N methanolic hydrochloric acid, 1.02 g of sodium cyanoborohydride and 75 ml of methanol is stirred and refluxed overnight. An additional 1.02 g of sodium cyanoborohydride is added and refluxing is continued for another day. The mixture is cooled, acidified to pH=1 with concentrated hydrochloric acid, the methanol is evaporated and the solution washed with diethyl ether. It is rendered basic to pH=10-11 with 3 N aqueous sodium hydroxide, extracted with diethyl ether, the extract dried and evaporated. The residue is recrystallized from hexane, to yield the 1-(2-isopropylaminopropyl)-9-methoxy-3-methyl-3,4,5,5a,6,7-hexahydro-2H-naphth[1,2-d]azepin-2-one melting at 118°-120°.

後処理

  1. temperaturerefluxed overnight
  2. temperaturerefluxing
  3. waitis continued for another day
  4. temperatureThe mixture is cooled
  5. customthe methanol is evaporated
  6. washthe solution washed with diethyl ether
  7. extractionextracted with diethyl ether
  8. customthe extract dried
  9. customevaporated
  10. customThe residue is recrystallized from hexane

出典と根拠

ORDレコード
ord-46335f8254dd4f04b6fdf084fb886a29
出典データセット
uspto-grants-1979_11
特許番号
US04173633

反応ノート

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