Simple exploration of 188937-16-8

The synthetic route of 188937-16-8 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.188937-16-8,2-(2-Thiazolyl)acetic Acid,as a common compound, the synthetic route is as follows.

To a solution of 5-bromo-4- (4-fluorophenyl) -6-hydrazinylpyrimidin-2-amine (400 mg, 1.3 mmol), 2- (1, 3-thiazol-2-yl) acetic acid (384 mg, 2.7 mmol), TEA (543 mg, 5.4 mmol) in DMSO (10 mL) was added HATU (1.3 g, 3.4 mmol). Stirred at 25C for 4 hours. The resulting mixture was poured into 100 mL water and filtered. The solid was dried in vacuum to afford N- [2-amino-5-bromo-6- (4-fluorophenyl) pyrimidin-4-yl]-2-(1, 3-thiazol-2-yl) acetohydrazide (336 mg, 59%) as a dark-grey solid. LCMS: m/z (ESI), [M+H] + = 423, 4. 1H NMR (300 MHz, DMSO-d 6) delta 4.05 (s, 2H), 6.42 (s, 2H), 7.28 (t, 2H), 7.54-7.70 (m, 3H), 7.75 (d, 1H), 8.75 (s, 1H), 10.22 (s, 1H)., 188937-16-8

The synthetic route of 188937-16-8 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; DIZAL (JIANGSU) PHARMACEUTICAL CO., LTD.; ZENG, Qingbei; QI, Changhe; TSUI, Honchung; YANG, Zhenfan; ZHANG, Xiaolin; (206 pag.)WO2020/52631; (2020); A1;,
Thiazole | C3H3NS – PubChem
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