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METHYL 2-AMINO-5-(4-FLUOROPHENYL)-1,3-THIAZOLE-4-CARBOXYLATE synthesis

1synthesis methods
-

Yield:-

Reaction Conditions:

in acetone at 57; for 24 h;

Steps:

A.1.5.2

A solution of the respective α-oxo-ester (22.1 mmol, 1.0 eq) in acetone (25 mL) is added to a suspension of thiourea (22.1 mmol, 1.0 eq) in acetone (45 mL). The mixture is heated to 57° C. (bath temperature), stirred for 24 h and concentrated to half of the volume. The obtained suspension is filtered and the residue is washed with acetone. After drying the desired amino-thiazole derivative is obtained as a solid.

References:

US2010/222328,2010,A1 Location in patent:Page/Page column 23