Share a compound : 37687-24-4

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Diethyl 3,5-pyrazoledicarboxylate, other downstream synthetic routes, hurry up and to see.

Adding a certain compound to certain chemical reactions, such as: 37687-24-4, name is Diethyl 3,5-pyrazoledicarboxylate, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 37687-24-4, COA of Formula: C9H12N2O4

A mixture of diethyl 1H-pyrazole-3,5-dicarboxylate (2.00 g, 9.42 mmol), 2-bromo-1-(3,4-dihydro-2/-/-chromen-2-yl)ethanone (Intermediate 209A, 2.52 g, 9.90 mmol) and potassium carbonate (1.43 g, 10.4 mmol) in dry acetone (50 ml) was stirred at RT overnight. After filtering off the solids, the filtrate was evaporated and the residue partitioned between dichloromethane and water. The organic phase was washed with water and brine, then dried over sodium sulfate and concen- trated. The residue was purified by flash-chromatography on silica gel (80 g, eluent: 0-25% ethyl acetate in petroleum ether) to give the title compound (2.88 g, 79% of theory). 1H-NMR (300 MHz, CDCIs): d [ppm] = 7.44 (s, 1H), 7.21-7.16 (m, 1H), 7.12-7.10 (m, 1H), 6.95- 6.90 (m, 2H), 5.95 (d, 1H), 5.69 (d, 1H), 4.75-4.71 (m, 1H), 4.42 (q, 2H), 4.30 (q, 2H), 2.88-2.82 (m, 2H), 2.36-2.17 (m, 2H), 1.40 (t, 3H), 1.35 (t, 3H).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, Diethyl 3,5-pyrazoledicarboxylate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; BAYER AKTIENGESELLSCHAFT; BAYER PHARMA AKTIENGESELLSCHAFT; MUeLLER, Steffen; SCHOHE-LOOP, Rudolf; ORTEGA, HERNANDEZ, Nuria; SUeSSMEIER, Frank; JIMENEZ NUNEZ, Eloisa; BRUMBY, Thomas; LINDNER, Niels; GERDES, Christoph; POOK, Elisabeth; BUCHMUeLLER, Anja; GAUGAZ, Fabienne, Zdenka; LANG, Dieter; ZIMMERMANN, Stefanie; EHRMANN, Alexander, Helmut, Michael; GERISCH, Michael; LEHMANN, Lutz; TIMMERMANN, Andreas; SCHAeFER, Martina; SCHMIDT, Georg; SCHLEMMER, Karl-Heinz; FOLLMANN, Markus; KERSTEN, Elisabeth; WANG, Vivian; GAO, Xiang; WANG, Yafeng; (801 pag.)WO2019/219517; (2019); A1;,
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics