2-Aminothiazole → HCID 9900454, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([N:8]=[C:9]=[S:10])[CH:7]=1.[NH2:12][C:13]1[S:14][CH:15]=[CH:16][N:17]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([NH:8][C:9]([NH:12][C:13]2[S:14][CH:15]=[CH:16][N:17]=2)=[S:10])[CH:7]=1Participants
3
Procedure
Prepared using Method C from 3.0 g (16.3 mmol) of 5-chloro-2-methyl-phenyl isothiocyanate and 1.7 g (16.3 mmol) of 2-amino-thiazole to give 3.58 g of title compound as a beige solid, m.p. 197-198° C. (77% yield).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-63170f59124b453795855cb6310a05c5
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06455566B1
Reaction notes
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