Hydrochloric Acid → Cinacalcet Hydrochloride

HRID 1296832Notes

Reaction equation

HRID 1296832 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]>CCCCCC>[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

Procedure

0.8 g of cinacalcet base was dissolved in 50 ml of n-hexane at room temperature. Then, HCl gas was bubbled into the solution, producing a precipitate. The HCl gas was added until no more precipitation was observed. The resulting slurry was stirred at room temperature for 20 minutes. The product was isolated by filtration, washed with 10 ml of n-Hexane, and dried at 50° C. in a vacuum oven for 17 hours, yielding 0.76 g of cinacalcet hydrochloride crystalline Form I.

Workup

  1. customThen, HCl gas was bubbled into the solution
  2. customproducing a precipitate
  3. customThe product was isolated by filtration
  4. washwashed with 10 ml of n-Hexane
  5. customdried at 50° C. in a vacuum oven for 17 hours

Sources & evidence

ORD record
ord-254ac81851ea40cb85743dc567c5eb5d
Source dataset
uspto-grants-2007_07
Patent number
US07247751B2

Reaction notes

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