Hydrochloric Acid → 1-{2-[4-(2-Hydroxy-2-methylpropyl)piperazin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethyl}cyclohexanol dihydrochloride

HRID 28840Notes

Reaction equation

HRID 28840 reaction equation
[OH:1][C:2]([CH3:31])([CH3:30])[CH2:3][N:4]1[CH2:9][CH2:8][N:7]([CH2:10][CH:11]([C:23]2([OH:29])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]2)[C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([O:18][C:19]([F:22])([F:21])[F:20])[CH:13]=2)[CH2:6][CH2:5]1.[ClH:32].C(OCC)C>CO>[ClH:32].[ClH:32].[OH:1][C:2]([CH3:31])([CH3:30])[CH2:3][N:4]1[CH2:9][CH2:8][N:7]([CH2:10][CH:11]([C:23]2([OH:29])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]2)[C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([O:18][C:19]([F:22])([F:21])[F:20])[CH:13]=2)[CH2:6][CH2:5]1

Participants

5

Procedure

(1-{2-[4-(2-hydroxy-2-methylpropyl)piperazin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethyl}cyclohexanol (30 mg) was dissolved in methanol (0.5 mL) and treated with a saturated methanolic solution of hydrochloric acid (0.5 mL) followed by diethyl ether. After crystallizing in the refrigerator for 16 h, the resulting solid was collected, washed with diethyl ether and dried in vacuo to yield 16 mg (54%) (1-{2-[4-(2-hydroxy-2-methylpropyl)piperazin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethyl}cyclohexanol dihydrochloride as a white solid. MS m/z 445; HRMS: calcd for C23H35F3N2O3+H+, 445.26725; found (ESI, [M+H]+), 445.268.

Workup

  1. customAfter crystallizing in the refrigerator for 16 h
  2. customthe resulting solid was collected
  3. washwashed with diethyl ether
  4. customdried in vacuo

Sources & evidence

ORD record
ord-38abb5a742744358836f92e014a39484
Source dataset
uspto-grants-2008_09
Patent number
US07419980B2

Reaction notes

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