Hydrochloric Acid → 1-(2-dimethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-4-phenylbutan-1-one hydrochloride
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:24][C:8]2[CH2:9][N:10]([C:13](=[O:23])[CH2:14][CH2:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3].[ClH:25]>CO.C(OCC)(=O)C>[ClH:25].[CH3:1][N:2]([CH2:4][C:5]1[O:24][C:8]2[CH2:9][N:10]([C:13](=[O:23])[CH2:14][CH2:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
1-(2-Dimethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-4-phenylbutan-1-one 0.161 g was dissolved in 2 ml of methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. After this mixture was concentrated, diethyl ether was added; the resulting solid was filtered and washed with diethyl ether to yield the desired product.
Workup
- concentrationAfter this mixture was concentrated
- additiondiethyl ether was added
- filtrationthe resulting solid was filtered
- washwashed with diethyl ether
Sources & evidence
- ORD record
- ord-3a03cb5889984fa29bde14e97cd765d2
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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