Water → HCID 18409092、化合物

HRID 1033508ノート

反応式

HRID 1033508 の反応式
[CH3:1][N:2](OCC1C=CC=CC=1)[C:3]1([CH3:21])[CH2:12][CH2:11][CH2:10][C:9]2[N:8]=[C:7]([O:13][CH2:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH:6]=[CH:5][C:4]1=2.B.O1CCCC1.O>O1CCCC1>[CH3:1][NH:2][C:3]1([CH3:21])[CH2:12][CH2:11][CH2:10][C:9]2[N:8]=[C:7]([O:13][CH2:14][C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:6]=[CH:5][C:4]1=2

参加物

5

反応条件

温度
0 °C

実験手順

5,6,7,8-Tetrahydro-N,5-dimethyl-N,2-bis(phenylmethoxy)-5-quinolinamine (12.3 g) in tetrahydrofuran (160 ml) at 0° C. was treated dropwise with borane-tetrahydrofuran complex (1M in tetrahydrofuran, 63.4 ml). The solution was heated under reflux for 3 hrs, cooled to 0° C., and water (30 ml) was added. The reaction mixture was concentrated in vacuo, 20% potassium hydroxide solution (60 ml) was added, and the mixture was heated at reflux for 2 hrs. The mixture was cooled, acidified with conc hydrochloric acid, and washed with diethyl ether. The aqueous phase was basified with 20% potassium hydroxide solution and extracted with dichloromethane. The combined organic layers were washed with brine, dried over potassium carbonate, filtered, and the filtrate was concentrated to afford 6.3 g (92%) of product.

後処理

  1. temperatureThe solution was heated
  2. temperatureunder reflux for 3 hrs
  3. concentrationThe reaction mixture was concentrated in vacuo, 20% potassium hydroxide solution (60 ml)
  4. additionwas added
  5. temperaturethe mixture was heated
  6. temperatureat reflux for 2 hrs
  7. temperatureThe mixture was cooled
  8. washwashed with diethyl ether
  9. extractionextracted with dichloromethane
  10. washThe combined organic layers were washed with brine
  11. dry with materialdried over potassium carbonate
  12. filtrationfiltered
  13. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-1e6a591bfa41458face4c738a924743c
出典データセット
uspto-grants-1994_05
特許番号
US05310914

反応ノート

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