Hydrochloric Acid → 1-Ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea hydrochloride
Reaction equation
[CH2:1]([O:3][C:4]([NH:6][C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH:16][C:17](=[O:22])[CH2:18][N:19]([CH3:21])[CH3:20])=[S:8])=[O:5])[CH3:2].[ClH:23]>C(O)C.C(OCC)C>[ClH:23].[CH2:1]([O:3][C:4]([NH:6][C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH:16][C:17](=[O:22])[CH2:18][N:19]([CH3:21])[CH3:20])=[S:8])=[O:5])[CH3:2]Participants
5
Procedure
1-Ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea (5.0 g) was dissolved in the minimum quantity of ethanol and the solution treated with diethyl ether (500 ml), followed by a saturated solution of hydrogen chloride in diethyl ether. The resultant solid was filtered off and recrystallised from ethanol/diethyl ether to give 1-ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea hydrochloride (4.3 g), m.p. 178°-180° C. (with decomposition).
Workup
- filtrationThe resultant solid was filtered off
- customrecrystallised from ethanol/diethyl ether
Sources & evidence
- ORD record
- ord-eb1be748e62f42b9af18701679b19d15
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04005217
Reaction notes
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