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ChemicalBook CAS DataBase List N-(2-Chloro-6-methylphenyl)-2-[(6-chloro-2-methyl-4-pyrimidinyl)amino]-5-thiazolecarboxamide
302964-08-5

N-(2-Chloro-6-methylphenyl)-2-[(6-chloro-2-methyl-4-pyrimidinyl)amino]-5-thiazolecarboxamide synthesis

11synthesis methods
1780-26-3 Synthesis
4,6-Dichloro-2-methylpyrimidine

1780-26-3
468 suppliers
$10.00/10g

302964-24-5 Synthesis
2-Amino-N-(2-chloro-6-methylphenyl)thiazole-5-carboxamide

302964-24-5
404 suppliers
$9.00/250mg

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Yield:302964-08-5 98.7%

Reaction Conditions:

with potassium hydride in tetrahydrofuran at -25 - -10; for 4 h;Reagent/catalyst;Temperature;

Steps:

1

To 80 ml of tetrahydrofuran cooled to -25 ° C, 8.73 g of potassium hydride (30% by weight, 65.38 mmol) was added; stirred and stirred for 10 min; slowly added to 5.00 g of 2-amino-N- (2-chloro- Phenyl) thiazole-5-carboxamide was added at a temperature of -25 ° C and a solution of 3.65 g of tetrahydrofuran (7 ml) containing 2-methyl-4,6-dichloropyrimidine was added in advance to a solution of In the reaction system, the temperature was stabilized and the reaction was stirred at -10 ° C for 4 hours. Then, ImoVL hydrochloric acid quenched reaction was slowly added. The pH was adjusted to 6, controlled at 0-5 ° C, crystallized for 2 h, centrifuged, washed with THF, The crude product was 7.27g. The yield was 98.7%, the purity was 99.95% (HPLC), and the maximum single hetero content was 0.03%

References:

CN104788445,2017,B Location in patent:Paragraph 0016; 0026; 0027; 0029; 0031; 0033; 0035; 0037

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