Hydrochloric Acid → HCID 20502541, compound
Reaction equation
C([N:20]1[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][N:29]2[C:39]3[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=3)[C:32](=[O:33])[C:30]2=[O:31])[CH2:22][CH2:21]1)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[ClH:40]>O1CCCC1>[ClH:40].[ClH:40].[N:23]1([CH2:26][CH2:27][CH2:28][N:29]2[C:39]3[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=3)[C:32](=[O:33])[C:30]2=[O:31])[CH2:24][CH2:25][NH:20][CH2:21][CH2:22]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1-[3-(4-trityl-1-piperazinyl)propyl]isatin (5.0 g) in tetrahydrofuran (100 ml) was added all at once concentrated hydrochloric acid (5 ml) and the mixture was vigorously stirred for half an hour. The resultant precipitates were collected by filtration and washed with tetrahydrofuran to give 1-[3-(1-piperazinyl)propyl]isatin dihydrochloride (2.96 g).
Workup
- customThe resultant precipitates
- filtrationwere collected by filtration
- washwashed with tetrahydrofuran
Sources & evidence
- ORD record
- ord-ebefe7087524460ea98363bdf557de33
- Source dataset
- uspto-grants-1983_05
- Patent number
- US04382934
Reaction notes
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