Hydrochloric Acid → (R)-8-Fluoro-3-(N-3-pentyl-N-n-propylamino)-5-trifluoromethanesulfonyloxychroman hydrochloride
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:21][S:22]([C:25]([F:28])([F:27])[F:26])(=[O:24])=[O:23])=[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:29]>CCOCC>[ClH:29].[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:21][S:22]([C:25]([F:27])([F:26])[F:28])(=[O:23])=[O:24])=[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]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(R)-8-Fluoro-3-(N-3-pentyl-N-n-propylamino)-5-trifluoromethanesulfonyloxychroman (100 mg, 0.23 mmol) was dissolved in ether. HCl in ether was added to precipitate the HCl-salt, and gave after drying 110 mg of (R)-8-fluoro-3-(N-3-pentyl-N-n-propylamino)-5-trifluoromethanesulfonyloxychroman hydrochloride as a white powder. Mp. 45°-60° C. (sinters).
Workup
- customto precipitate the HCl-salt
- customgave
- dry with materialafter drying 110 mg of (R)-8-fluoro-3-(N-3-pentyl-N-n-propylamino)-5-trifluoromethanesulfonyloxychroman hydrochloride as a white powder
Sources & evidence
- ORD record
- ord-135b054ca91c4f45b44689b3d055fb5c
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05650524
Reaction notes
Loading…