Sources of common compounds: 330786-24-8

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 330786-24-8, 3-(4-Phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine.

Electric Literature of 330786-24-8, 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 330786-24-8, name is 3-(4-Phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine. This compound has unique chemical properties. The synthetic route is as follows.

3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (100.00 mg, 329.68 mumol) was weighed in a single-mouth flask and anhydrous tetrahydrofuran (10 ml) was added. , Triphenylphosphine (259.42mg, 989.04mumol) was added under argon protection.(S)-3-(4-hydroxyphenyl)-1-(piperidin-1-yl)prop-2-en-1-one (51.17 mg, 329.68 mumol), Diethyl azodicarboxylate (199.99 Mg, 989.04 [mu]mol), overnight at room temperature, complete reaction monitored by TLC. The reaction solution was concentrated and column chromatography afforded BTK-187 mg in a yield of 83.65%.

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 330786-24-8, 3-(4-Phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine.

Reference:
Patent; Shanghai Institute of Technology; Yao Zhiyi; Yang Yan; Xia Xiaoming; Xue Nannan; Shu Qisheng; Wang Qingxuan; Wang Dongsheng; (7 pag.)CN107827892; (2018); A;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia