Hydrochloric Acid → (R)-8-Fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman hydrochloride
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([OH:21])=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])[CH2:7]2.[ClH:22]>CCOCC>[ClH:22].[F:1][C:2]1[CH:3]=[CH:4][C:5]([OH:21])=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:17][CH3:18])[CH2:19][CH3:20])[CH2:13][CH2:14][CH3:15])[CH2:7]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(R)-8-Fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman (180 mg, 0.6 mmol) was dissolved in ether. HCl in ether was added to precipitate the HCl-salt, and gave after drying 200 mg of (R)-8-fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)-chroman hydrochloride as a white powder. Mp: 80°-100° C. (sinters).
Workup
- customto precipitate the HCl-salt
- customgave
- dry with materialafter drying 200 mg of (R)-8-fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)-chroman hydrochloride as a white powder
Sources & evidence
- ORD record
- ord-8cacfe3a3ebb4d3eb449d138178fa93f
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05420151
Reaction notes
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