Hydrochloric Acid → HCID 68497645, compound
Reaction equation
[CH3:1][C@@:2]12[CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C@:3]1([CH3:15])[NH:4][CH2:5][CH2:6][CH2:7]2.[ClH:16]>>[ClH:16].[CH3:1][C@@:2]12[CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C@:3]1([CH3:15])[NH:4][CH2:5][CH2:6][CH2:7]2Participants
3
Procedure
(−)-(4aR*,9bR*)-4a,9b-Dimethyl-2,3,4,4a,5,9b-hexahydro-1H-indeno[1,2-b]pyridine and (+)-(4aR*,9bR*)-4a,9b-dimethyl-2,3,4,4a,5,9b-hexahydro-1H-indeno[1,2-b]pyridine were each made into a hydrochloride by a conventional method, washed with ethyl acetate, and then collected by filtration to obtain (4aR*,9bR*)-4a,9b-dimethyl-2,3,4,4a,5,9b-hexahydro-1H-indeno[1,2-b]pyridine hydrochloride and an enantiomer thereof, respectively, as a colorless powder.
Workup
- washwashed with ethyl acetate
- filtrationcollected by filtration
Sources & evidence
- ORD record
- ord-09b727cd9fe646e0ac647f229b7b13a6
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08211907B2
Reaction notes
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