Hydrochloric Acid → HCID 67585989, compound
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:28][C:8]2[CH2:9][N:10]([C:13]([C:15]3[S:16][C:17](/[CH:20]=[CH:21]\[C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)=[CH:18][CH:19]=3)=[O:14])[CH2:11][CH2:12][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:28][C:8]2[CH2:9][N:10]([C:13]([C:15]3[S:16][C:17](/[CH:20]=[CH:21]\[C:22]4[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=4)=[CH:18][CH:19]=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
(Z)-N,N-Dimethyl-[6-[5-(2-phenylethenyl)thiophene-2-carbonyl]-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 0.157 g was dissolved in methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. This mixture was concentrated, and recrystallized from methanol-diethyl ether to yield the desired product.
Workup
- concentrationThis mixture was concentrated
- customrecrystallized from methanol-diethyl ether
Sources & evidence
- ORD record
- ord-f7383f3792a04950884b596dfacfc663
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
Loading…