Hydrochloric Acid → HCID 19923139, compound
Reaction equation
O1CCCC1.[CH2:6]([O:20][C:21]1[CH:26]=[CH:25][C:24]([CH2:27][C:28]([NH:30][C:31]2[CH:36]=[CH:35][CH:34]=[C:33]([CH2:37][C:38]3[S:39][CH:40]=[CH:41][N:42]=3)[CH:32]=2)=[O:29])=[CH:23][CH:22]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].[ClH:43]>CCOCC>[ClH:43].[CH2:6]([O:20][C:21]1[CH:22]=[CH:23][C:24]([CH2:27][C:28]([NH:30][C:31]2[CH:36]=[CH:35][CH:34]=[C:33]([CH2:37][C:38]3[S:39][CH:40]=[CH:41][N:42]=3)[CH:32]=2)=[O:29])=[CH:25][CH:26]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a tetrahydrofuran:ether solution of 4-(tetradecyloxy)-N-[3-(2-thiazolylmethyl)phenyl]benzeneacetamide is added ether saturated with hydrogen chloride. The resulting solid is collected by centrifugation and dried in vacuum to give 0.18 g of the desired product as a tan solid, m.p. 155°-158° C.
Workup
- customThe resulting solid is collected by centrifugation
- customdried in vacuum
Sources & evidence
- ORD record
- ord-35f18908af9845139f21a7edf82d7a28
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05128351
Reaction notes
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