Hydrochloric Acid → HCID 11186350, compound
Reaction equation
C(OC([N:8]1[CH2:26][C@@H:25]([CH3:27])[N:11]2[C:12](=[O:24])[C:13]3[C:18]([C@@H:10]2[CH2:9]1)=[CH:17][CH:16]=[CH:15][C:14]=3[O:19][C:20]([F:23])([F:22])[F:21])=O)(C)(C)C.[ClH:28]>CCOCC.O>[ClH:28].[CH3:27][C@H:25]1[N:11]2[C:12](=[O:24])[C:13]3[C:18]([C@@H:10]2[CH2:9][NH:8][CH2:26]1)=[CH:17][CH:16]=[CH:15][C:14]=3[O:19][C:20]([F:23])([F:22])[F:21]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirring solution of N-(t-butoxycarbonyl)-(4R,10bR)-1,3,4,10b-tetrahydro-4-methyl-7-trifluoromethoxy-pyrazino[2,1-a]isoindol-6(2H)-one(30 mg, 0.08 mmol) in dry ether (2 mL) was added hydrochloric acid (1 mL). The reaction was stirred for 1 h and then conc. in vacuo to a white solid. The solid was dissolved in water and lyophilized to 21 mg of a white solid. MS (ESI) 271 (M−Cl).
Sources & evidence
- ORD record
- ord-3036a5f3e4ba477aa8a1685d6539287c
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07244843B2
Reaction notes
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