Hydrochloric Acid → N-[2-[4-(6-Fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride

HRID 233221Notes

Reaction equation

HRID 233221 reaction equation
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([N:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][N:19]4[C:23](=[O:24])[C:22]5=[CH:25][CH:26]=[CH:27][CH:28]=[C:21]5[C:20]4=[O:29])[CH2:13][CH2:12]3)=[N:7][NH:8]2)=[CH:4][CH:3]=1.[ClH:30].CCOCC>CO>[ClH:30].[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([N:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][N:19]4[C:23](=[O:24])[C:22]5=[CH:25][CH:26]=[CH:27][CH:28]=[C:21]5[C:20]4=[O:29])[CH2:13][CH2:12]3)=[N:7][NH:8]2)=[CH:4][CH:3]=1

Participants

5

Procedure

A 5.0 g sample of N-[2-[4-(6-fluoro-1 H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide was suspended in methanol (130 ml) and was made acidic with ethereal-HCl. After stirring for 1 hour, anhydrous ether (100 ml) was added and the suspension was stirred for an additional 30 minutes. The solid was collected and dried to afford 4.5 g of an off-white powder. This was combined with an additional sample (7.3 g total) and recrystallization from MeOH gave 4.3 g of the salt as an off-white powder, mp=265°-268° C.

Workup

  1. stirringthe suspension was stirred for an additional 30 minutes
  2. customThe solid was collected
  3. customdried

Sources & evidence

ORD record
ord-51dc4c6dd1ec4788bd079928d60a4d35
Source dataset
uspto-grants-1997_01
Patent number
US05591745

Reaction notes

Loading…