Hydrochloric Acid → 5,6-Dihydro-N,N-dimethyl-6-phenyl-11H-pyrido[2,3-b][1,4]benzodiazepine-11-propanamine, dihydrochloride hemihydrate

HRID 543628

反応式

HRID 543628 の反応式
[CH3:1][N:2]([CH3:27])[CH2:3][CH2:4][CH2:5][N:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:9][C:8]2[CH:23]=[CH:24][CH:25]=[N:26][C:7]1=2.[ClH:28].[BH3-]C#N.[Na+].C[OH:34]>>[OH2:34].[ClH:28].[ClH:28].[CH3:27][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][N:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[NH:9][C:8]2[CH:23]=[CH:24][CH:25]=[N:26][C:7]1=2.[CH3:27][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][N:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[NH:9][C:8]2[CH:23]=[CH:24][CH:25]=[N:26][C:7]1=2.[ClH:28].[ClH:28]

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 54961TampramineHCID 5003444Sodium cyanoborohydride

生成物 1

HCID 704878055,6-Dihydro-N,N-dimethyl-6-phenyl-11H-pyrido[2,3-b][1,4]benzodiazepine-11-propanamine, dihydrochloride hemihydrate

実験手順

A solution of 3.0 g (0.0064 mole) of N,N-dimethyl-6-phenyl-11H-pyrido[2,3-b][1,4]benzodiazepine-11-propanamine in absolute methanol was adjusted to pH 5.6 with methanolic hydrogen chloride solution. To this solution was added at one time, 0.7 g (0.011 mole) of NaBH3CN and the reaction mixture was refluxed for 20 min. The ethanol was removed in vacuo and the residue was partitioned between dilute sodium hydroxide and methylene chloride. The methylene chloride layer was dried over magnesium sulfate and concentrated to leave a residue which was twice crystallized from 2-propanol and isopropyl ether. A yellow solid, 1.6 g (57%) was obtained which loses its crystalline structure on heating starting at 156°-160° C. with decomposition at 180°-195° C.

後処理

  1. temperaturethe reaction mixture was refluxed for 20 min
  2. customThe ethanol was removed in vacuo
  3. customthe residue was partitioned between dilute sodium hydroxide and methylene chloride
  4. dry with materialThe methylene chloride layer was dried over magnesium sulfate
  5. concentrationconcentrated
  6. customto leave a residue which
  7. customwas twice crystallized from 2-propanol and isopropyl ether
  8. customA yellow solid, 1.6 g (57%) was obtained which
  9. temperatureon heating
  10. customstarting at 156°-160° C. with decomposition at 180°-195° C.

出典と根拠

ORDレコード
ord-bcb7c7b0a59b407a9512e3619e356d62
出典データセット
uspto-grants-1984_05
特許番号
US04447361

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