Sources of common compounds: 934524-10-4

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 934524-10-4, 2,4-Dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine.

Electric Literature of 934524-10-4, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 934524-10-4, name is 2,4-Dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine. This compound has unique chemical properties. The synthetic route is as follows.

General procedure: To a solution of S2a (142mg, 0.415mmol) in nBuOH (4mL) was added DIPEA (67mg, 0.5187mmol) and 2-methoxyethylamine (37mg, 0.4980mmol). The mixture was stirred at 50C for 1 hr until starting material was consumed at which point the reaction was allowed to cool to rt and the nBuOH was removed under reduced pressure. The resulting residue was taken up in EtOAc and washed with saturated NH4Cl. The organic layer was isolated, dried over MgSO4, and concentrated under reduced pressure to yield 2-chloro-N-(2-methoxyethyl)-5-(p-tolylsulfonyl)pyrrolo[3,2-d]pyrimidin-4-amine (S3a) as a solid (100mg, 63% yield).

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 934524-10-4, 2,4-Dichloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine.

Reference:
Article; Wormald, Michael M.; Ernst, Glen; Wei, Huijun; Barrow, James C.; Bioorganic and Medicinal Chemistry Letters; vol. 29; 19; (2019);,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia