Hydrochloric Acid → HCID 131716676, compound

HRID 1587792Notes

Reaction equation

HRID 1587792 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][C:15]([N:17]3[CH2:22][CH:21]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([F:32])([F:31])[F:30])[CH:24]=4)[N:19]4[N:33]=[CH:34][C:35]([C:36]#[N:37])=[C:18]34)=[O:16])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[ClH:38].CCOCC>C(OCC)(=O)C>[ClH:38].[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][C:15]([N:17]3[CH2:22][CH:21]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([F:31])([F:30])[F:32])[CH:24]=4)[N:19]4[N:33]=[CH:34][C:35]([C:36]#[N:37])=[C:18]34)=[O:16])[CH2:10][CH2:9]2)=[CH:6][CH:7]=1

Participants

5

Procedure

A 6.6 g portion of 4-[[4-(4-fluorophenyl)-1-piperazinyl]acetyl]-4,5-dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile was heated to solution in 100 ml of ethyl acetate, then cooled and acidified with 25 ml of 2.44N ethanolic hydrochloric acid. Ether was added, the solid collected, heated to boiling in 500 ml of ethanol, then cooled and the crystalline salt collected, giving 5.7 g of the desired product, mp 242°-244° C.

Workup

  1. temperaturecooled
  2. customthe solid collected
  3. temperatureheated
  4. temperaturecooled
  5. customthe crystalline salt collected

Sources & evidence

ORD record
ord-297889d524034264857d6773645cb843
Source dataset
uspto-grants-1993_06
Patent number
US05219857

Reaction notes

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