With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.40283-41-8,2-Aminothiazole-4-carboxylic acid,as a common compound, the synthetic route is as follows.
To a solution of (+/-)-cis-N?-(2-(5,7-difluoro-1-tosyl-1H-indol-3-yl)-6-phenylpyrimidin-4-yl)cyclohexane- 1,3 -diamine (50 mg, 0.09 mmol) and2-aminothiazole-4-carboxylic acid (27 mg, 0.19 mmol) in a mixed solvent of dimethyl sulfoxide (2 mL) and tetrahydrofuran (4 mL) was added DIPEA (46 1iL, 0.28 mmol).The mixture was stirred at rt for 10 mm then HATU (68 mg, 0.18 mmol) was added. The resulting mixture was stirred at rt overnight. To the reaction mixture was added water (30 mL), and the mixture was exttracted with ethyl acetate (30 mL x 3). The combined organic layers were washed with a saturated aqueous sodium chloride solution(60 mL), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated in vacuo to give the title compound as a light yellow solid (89 mg), which was used in the next step without further purification.
40283-41-8, As the paragraph descriping shows that 40283-41-8 is playing an increasingly important role.
Reference：
Patent; SUNSHINE LAKE PHARMA CO., LTD.; REN, Qingyun; TANG, Changhua; YIN, Junjun; YI, Kai; ZHANG, Yingjun; (264 pag.)WO2018/33082; (2018); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica