Hydrochloric Acid → 76906-72-4
Reaction equation
C([C:9]1[C:14]([OH:15])=[CH:13][N:12]=[C:11]([CH2:16][CH:17]([NH:19][CH:20]([CH3:22])[CH3:21])[CH3:18])[C:10]=1C(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.[ClH:31]>>[ClH:31].[ClH:31].[CH:20]([NH:19][CH:17]([CH3:18])[CH2:16][C:11]1[CH:10]=[CH:9][C:14]([OH:15])=[CH:13][N:12]=1)([CH3:22])[CH3:21]Participants
3
Procedure
Similarly, the mixture of 0.1 g of dibenzoyl-2-(2-isopropylaminopropyl)-5-pyridinol and 10 ml of 5 N hydrochloric acid may be refluxed for three days, cooled, filtered, evaporated and the residue triturated with acetone, to yield the 2-(2-isopropylaminopropyl)-5-pyridinol dihydrochloride melting at 199°-204°; it is identical with that obtained according to Examples 1, 3 and 8.
Workup
- temperaturemay be refluxed for three days
- temperaturecooled
- filtrationfiltered
- customevaporated
- customthe residue triturated with acetone
Sources & evidence
- ORD record
- ord-8f1d4ecba30d442289c8d990dad58f88
- Source dataset
- uspto-grants-1981_04
- Patent number
- US04260619
Reaction notes
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