Hydrochloric Acid → Atomoxetine hydrochloride
Reaction equation
[ClH:1].[CH3:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][C@@H:10]([C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)[CH2:11][CH2:12][NH:13][CH3:14]>>[CH3:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][C@@H:10]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:11][CH2:12][NH:13][CH3:14].[ClH:1]Participants
3
Procedure
Under stirring, and maintaining temperature between 18° C. and 20° C. by means of water bath cooling, 3.27 g (0.03263 mol) of aqueous hydrogen chloride (36.4%) was dropped on 58.2 g (0.02967 mol) of the atomoxetine base solution obtained above. Atomoxetine hydrochloride then crystallized out. The obtained suspension was stirred at about 20° C. for one hour, the solid is collected by filtration, and washed twice with 6 ml of n-butyl acetate. The solid was collected and dried for 18 hours at 45° C. under vacuum.
Workup
- temperaturemaintaining temperature between 18° C. and 20° C. by means of water bath
- temperaturecooling
- customobtained above
- customAtomoxetine hydrochloride then crystallized out
- stirringThe obtained suspension was stirred at about 20° C. for one hour
- filtrationthe solid is collected by filtration
- washwashed twice with 6 ml of n-butyl acetate
- customThe solid was collected
- customdried for 18 hours at 45° C. under vacuum
Sources & evidence
- ORD record
- ord-b5f5f8d6c3a742a4bd5b3dbc5d1c308a
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07439399B2
Reaction notes
Loading…