Hydrochloric Acid → N,N-diethyl-[6-(4-phenylbutoxycarbonyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine hydrochloride
Reaction equation
[CH2:1]([N:3]([CH2:6][C:7]1[O:28][C:10]2[CH2:11][N:12]([C:15]([O:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[O:16])[CH2:13][CH2:14][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2].[ClH:29]>CO>[ClH:29].[CH2:1]([N:3]([CH2:6][C:7]1[O:28][C:10]2[CH2:11][N:12]([C:15]([O:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)=[O:16])[CH2:13][CH2:14][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N,N-Diethyl-[6-(4-phenylbutoxycarbonyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 0.198 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol was added in excess, followed by stirring. This reaction mixture was concentrated to yield the desired product.
Workup
- concentrationThis reaction mixture was concentrated
Sources & evidence
- ORD record
- ord-ffb97f4ac64d4c288314d4689a8f4890
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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