Hydrochloric Acid → 1-[(3,4-Dimethoxyphenyl)-2-propyl]amino-3-(1-naphthyloxy)propan-2-ol

HRID 374532Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 374532
[NH2:1][C@H:2]([CH3:14])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6]([O:12][CH3:13])[CH:5]=1.C[Si](C)(C)NC(=O)C.[C:23]1([O:33][CH2:34][CH:35]2[O:37][CH2:36]2)[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH:26]=[CH:25][CH:24]=1.Cl.[OH-].[Na+]>CS(C)=O>[CH3:13][O:12][C:6]1[CH:5]=[C:4]([CH2:3][CH:2]([NH:1][CH2:36][CH:35]([OH:37])[CH2:34][O:33][C:23]2[C:32]3[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=3)[CH:26]=[CH:25][CH:24]=2)[CH3:14])[CH:9]=[CH:8][C:7]=1[O:10][CH3:11]

Komponenten

7

Versuchsvorschrift

A mixture of 4.20 g of (R)-2-Amino-1-(3,4-dimethoxyphenyl)propane and 3.11 g of N-(trimethylsilyl)acetamide in 20 ml of dimethylsulfoxide is stirred at room temperature for 1 hour. A solution of 4.05 g of (1-naphthyl)glycidyl ether in 3 ml of dimethylsulfoxide is added to the above mixture and the resulting mixture is heated at 65° C. to 70° C. for 20 hours, cooled, poured into a mixture of ice and concentrated hydrochloric acid, stirred, basified with 10N sodium hydroxide and extracted with ethyl acetate. The ethyl acetate extract is washed with brine, dried, filtered and evaporated to yield 1-[(3,4-dimethoxyphenyl)-2-propyl]amino-3-(1- naphthyloxy)propan-2-ol.

Aufarbeitung

  1. temperaturethe resulting mixture is heated at 65° C. to 70° C. for 20 hours
  2. temperaturecooled
  3. stirringstirred
  4. extractionextracted with ethyl acetate
  5. extractionThe ethyl acetate extract
  6. washis washed with brine
  7. customdried
  8. filtrationfiltered
  9. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-762f2c25e3704937938ec1b6355b3e56
Quelldatensatz
uspto-grants-1996_01
Patentnummer
US05480908

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