Diethyl Ether → HCID 86628562, compound
Reaction equation
[C:1]1([C@H:11]([NH:13][CH2:14][C@H:15]2[C@H:19]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:18][N:17]([C:26](=[O:31])[C:27]([F:30])([F:29])[F:28])[CH2:16]2)[CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[ClH:32].C(OCC)(=O)C.C(OCC)C>C(OCC)(=O)C>[ClH:32].[C:1]1([C@H:11]([NH:13][CH2:14][C@H:15]2[C@H:19]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH2:18][N:17]([C:26](=[O:31])[C:27]([F:28])([F:29])[F:30])[CH2:16]2)[CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A 470 mg portion of (1R)-1-(1-naphthyl)-N-{[(3R,4R)-4-phenyl-1-(trifluoroacetyl)pyrrolidin-3-yl]methyl}ethanamine was dissolved in 8 ml of ethyl acetate and treated with 4 M hydrogen chloride/ethyl acetate solution. Diethyl ether was added to the reaction solution, and the thus precipitated crystals were recrystallized from ethyl acetate and diethyl ether to obtain 258 mg of (1R)-1-(1-naphthyl)-N-{[(3R,4R)-4-phenyl-1-(trifluoroacetyl)pyrrolidin-3-yl]methyl}ethanamine hydrochloride as colorless crystals.
Workup
- customthe thus precipitated crystals were recrystallized from ethyl acetate and diethyl ether
Sources & evidence
- ORD record
- ord-504a04828cd64061bdac4322e89c8330
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585886B2
Reaction notes
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