Hydrochloric Acid → HCID 19600037, compound
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:13][C:12]2[CH2:11][CH2:10][N:9]([C:14](=[O:28])[CH2:15][CH2:16][CH2:17][CH2:18][S:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)(=[O:21])=[O:20])[CH2:8][C:7]=2[CH:6]=1)[CH3:3].[ClH:29]>CO.C(OCC)(=O)C>[ClH:29].[CH3:1][N:2]([CH2:4][C:5]1[O:13][C:12]2[CH2:11][CH2:10][N:9]([C:14](=[O:28])[CH2:15][CH2:16][CH2:17][CH2:18][S:19]([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)(=[O:21])=[O:20])[CH2:8][C:7]=2[CH:6]=1)[CH3:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
1-(2-Dimethylaminomethyl-6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-5-phenylsulfonylpentan-1-one 0.081 g was dissolved in 2 ml of methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. This mixture was concentrated to yield the desired product.
Workup
- concentrationThis mixture was concentrated
Sources & evidence
- ORD record
- ord-f1cfbc38fd7d454d83a3cbca4b371095
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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