Hydrochloric Acid → N-(4-diethylamino-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide hydrochloride
Reaction equation
[CH2:1]([N:3]([CH2:25][CH3:26])[CH2:4][C:5]#[C:6][CH2:7][NH:8][C:9](=[O:24])[C:10]([CH:18]1[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1)([OH:17])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:2].[ClH:27]>C(Cl)(Cl)Cl>[ClH:27].[CH2:25]([N:3]([CH2:1][CH3:2])[CH2:4][C:5]#[C:6][CH2:7][NH:8][C:9](=[O:24])[C:10]([CH:18]1[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]1)([OH:17])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:26]Participants
4
Procedure
To a solution of N-(4-diethylamino-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide (74 mg) in chloroform was added 4.1N methanolic hydrogen chloride (0.2 ml) and the mixture was evaporated in vacuo to give N-(4-diethylamino-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide hydrochloride (90 mg) as oil.
Workup
- customthe mixture was evaporated in vacuo
Sources & evidence
- ORD record
- ord-90d3c527373b40eb99d5396d2347ac0d
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05066680
Reaction notes
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