Hydrochloric Acid → 1-[(1,2,3,4-Tetrahydro-1-oxo-2-naphthalenyl)-methyl]-4-anilino isonipecotamide, hydrochloride
Reaction equation
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH2:4][CH:3]1[CH2:12][N:13]1[CH2:21][CH2:20][C:16]([NH:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)([C:17]([NH2:19])=[O:18])[CH2:15][CH2:14]1.[ClH:29]>C(O)C>[ClH:29].[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH2:4][CH:3]1[CH2:12][N:13]1[CH2:21][CH2:20][C:16]([NH:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)([C:17]([NH2:19])=[O:18])[CH2:15][CH2:14]1Participants
4
Procedure
Finely-ground 1-[(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-methyl]-4-anilino isonipecotamide (5.0 g) is slurried in absolute ethanol and treated with 1.2 equivalents of ethereal hydrogen chloride. The resulting mixture is cooled and filtered to yield the title compound.
Workup
- temperatureThe resulting mixture is cooled
- filtrationfiltered
Sources & evidence
- ORD record
- ord-2bc12515b42e4c3983136af42078d2b0
- Source dataset
- uspto-grants-1977_09
- Patent number
- US04051248
Reaction notes
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