Hydrochloric Acid → Cinacalcet Hydrochloride
Reaction equation
[CH3:1][C@@H:2]([NH:13][CH2:14][CH2:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:22]=1)[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=12.[ClH:27]>C1(C)C=CC=CC=1>[CH3:1][C@@H:2]([NH:13][CH2:14][CH2:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[C:21]([C:23]([F:24])([F:25])[F:26])[CH:22]=1)[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=12.[ClH:27]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.49 g cinacalcet base was dissolved in 10 ml of toluene at room temperature, i.e., about 20° to about 25° C. Then, 2 ml of 1N HCl was added in one portion, and the resulting mixture was stirred at room temperature overnight, yielding a precipitate. The product was isolated by filtration, washed with 10 ml of toluene, and dried at 50° C. in a vacuum oven for 17 hours, yielding 0.02 g of cinacalcet hydrochloride crystalline Form I.
Workup
- customi.e., about 20° to about 25° C
- customyielding a precipitate
- customThe product was isolated by filtration
- washwashed with 10 ml of toluene
- customdried at 50° C. in a vacuum oven for 17 hours
Sources & evidence
- ORD record
- ord-a4e1f15bd8ae403793a31dd2356f464e
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07247751B2
Reaction notes
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