Hydrochloric Acid → HCID 19600080, compound
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:26][C:8]2[CH2:9][N:10]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:11][CH2:12][CH2:13][C:7]=2[CH:6]=1)[CH3:3].[ClH:27]>CO>[ClH:27].[ClH:27].[CH3:1][N:2]([CH2:4][C:5]1[O:26][C:8]2[CH2:9][N:10]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH2:11][CH2:12][CH2:13][C:7]=2[CH:6]=1)[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N,N-Dimethyl-[7-(6-phenylhexyl)-5,6,7,8-tetrahydro-4H-furo[2,3-c]azepin-2-ylmethyl]amine 0.739 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol 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-2a699fa9cb28490f865ea427650e4ca4
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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