Hydrochloric Acid → HCID 19599894, compound
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:29][C:8]2[CH2:9][N:10]([C:13]([C:15]3[CH:20]=[CH:19][C:18](/[CH:21]=[CH:22]/[C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)=[CH:17][CH:16]=3)=[O:14])[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3].[ClH:30]>CO.C(OCC)(=O)C>[ClH:30].[CH3:1][N:2]([CH2:4][C:5]1[O:29][C:8]2[CH2:9][N:10]([C:13]([C:15]3[CH:16]=[CH:17][C:18](/[CH:21]=[CH:22]/[C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=4)=[CH:19][CH:20]=3)=[O:14])[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
(E)-N,N-Dimethyl-[6-(4-stilbenecarbonyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 0.153 g was dissolved in 2 ml of methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. This mixture was concentrated; the resulting solid was washed with diethyl ether to yield the desired product.
Workup
- concentrationThis mixture was concentrated
- washthe resulting solid was washed with diethyl ether
Sources & evidence
- ORD record
- ord-2579057d46294c2a84234524e744758d
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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