Hydrochloric Acid → HCID 20439028, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12](=[O:13])[CH2:11][S:10][CH:9]2[C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)=[CH:4][CH:3]=1.Cl>C(OCC)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:12](=[O:13])[CH2:11][S:10][CH:9]2[C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1.5 g. of 3-(4-chlorophenyl)-2-(3-pyridyl)-4-thiazolidinone (Example 19, supra) in ethyl ether was prepared, cooled, and saturated with anhydrous hydrogen chloride. The solid material which precipitated was filtered off and identified by NMR spectrum as 3-(4-chlorophenyl)-2-(3-pyridyl)-4-thiazolidinone hydrochloride.
Workup
- temperaturecooled
- customThe solid material which precipitated
- filtrationwas filtered off
Sources & evidence
- ORD record
- ord-8341dbcce4304bbfbf2ce1a3fbb6aaac
- Source dataset
- uspto-grants-1984_11
- Patent number
- US04482712
Reaction notes
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