1,1-Dimethyl-2-thiourea → HCID 20551598, compound
Reaction equation
Cl[CH2:2][C:3]([C:5]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:6]=1[OH:12])=O.[CH3:13][N:14]([CH3:18])[C:15]([NH2:17])=[S:16]>>[CH3:13][N:14]([CH3:18])[C:15]1[S:16][CH:2]=[C:3]([C:5]2[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:6]=2[OH:12])[N:17]=1Participants
3
Procedure
17.5 g or 2-chloroacetyl-4-methylphenol and 10.9 g of N,N-dimethyl thiourea are heated for 20 minutes to 110° C. After cooling, the solidified mass is recrystallised from aqueous methanol, affording 14.2 g (96% of theory) of 2-dimethylamino-4-(2'-hydroxy-5'-methylphenyl)-thiazole of the formula (101) ##STR13## with a melting point of 108°-110° C.
Workup
- temperatureAfter cooling
- customthe solidified mass is recrystallised from aqueous methanol
Sources & evidence
- ORD record
- ord-3e49de8fbcf842fea08783f43e9575ff
- Source dataset
- uspto-grants-1982_02
- Patent number
- US04316036
Reaction notes
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