Hydrochloric Acid → N-(4-dimethylamino-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide hydrochloride

HRID 973987Notes

Reaction equation

HRID 973987 reaction equation
[CH3:1][N:2]([CH3:24])[CH2:3][C:4]#[C:5][CH2:6][NH:7][C:8](=[O:23])[C:9]([CH:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1)([OH:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[ClH:25]>CO>[ClH:25].[CH3:24][N:2]([CH3:1])[CH2:3][C:4]#[C:5][CH2:6][NH:7][C:8](=[O:23])[C:9]([CH:17]1[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]1)([OH:16])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1

Participants

4

Procedure

To a solution of N-(4-dimethylamino-2-butynyl)-2-cyclohexyl-2-hydroxy-2-phenylacetamide 0.48 g) in methanol (5 ml) was added 6.4N methanolic hydrogen chloride (1.5 ml) and the solution was evaporated in vacuo. The oily residue was crystallized from a mixture of isopropyl alcohol and ethyl acetate to give N-(4-dimethylamino-2-butynyl)-2-cyclohexyl-2-hydroxy-2phenylacetamide hydrochloride (0.3 g).

Workup

  1. customthe solution was evaporated in vacuo
  2. customThe oily residue was crystallized from a mixture of isopropyl alcohol and ethyl acetate

Sources & evidence

ORD record
ord-4fb0e42675e547e298bf7e343860ef6d
Source dataset
uspto-grants-1991_11
Patent number
US05066680

Reaction notes

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