Hydrochloric Acid → HCID 68497344, compound
Reaction equation
[CH2:1]([C@@:3]12[CH2:15][C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C@@H:4]1[NH:5][CH2:6][CH2:7][CH2:8]2)[CH3:2].[ClH:16]>>[ClH:16].[CH2:1]([C@@:3]12[CH2:15][C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C@@H:4]1[NH:5][CH2:6][CH2:7][CH2:8]2)[CH3:2]Participants
3
Procedure
(−)-(4aR*,9bR*)-4a-Ethyl-2,3,4,4a,5,9b-hexahydro-1H-indeno[1,2-b]pyridine and (+)-(4aR*,9bR*)-4a-ethyl-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-ethyl-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-d3d75a09580f499dbccc4a73641f17b8
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08211907B2
Reaction notes
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