Can You Really Do Chemisty Experiments About 479195-19-2

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 479195-19-2, help many people in the next few years.Safety of 2-Oxa-8-azaspiro[4.5]decane hydrochloride

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Safety of 2-Oxa-8-azaspiro[4.5]decane hydrochloride, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 479195-19-2, Name is 2-Oxa-8-azaspiro[4.5]decane hydrochloride, molecular formula is C8H16ClNO. In a Patent, authors is £¬once mentioned of 479195-19-2

4-quinazoline amine derivatives and their use (by machine translation)

A 4-quinazoline amine derivative as represented by formula (1), a pharmaceutical composition comprising the derivative, and an application thereof in preparing medicine for curing cancer. The cancer is a drug-resistant cancer, preferably a cancer resisting an EGFR reversible inhibitor, and more preferably, a cancer resisting gefitinib, erlotinib or lapatinib; alternatively, the cancer carries EGFR mutation.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 479195-19-2, help many people in the next few years.Safety of 2-Oxa-8-azaspiro[4.5]decane hydrochloride

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H10763N – PubChem

 

Simple exploration of 479195-19-2

479195-19-2, 479195-19-2 2-Oxa-8-azaspiro[4.5]decane hydrochloride 21955264, apiperidines compound, is more and more widely used in various fields.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.479195-19-2,2-Oxa-8-azaspiro[4.5]decane hydrochloride,as a common compound, the synthetic route is as follows.

To a solution 2-oxa-8-azaspiro[4.5]decane, HC1 (1 g, 5.63 mmol) and DIEA (2.9 mL, 16.9 mmol) in anhydrous CH3CN (35 mL) was added isopropyl 2-(5-bromo-4- chloro-2,6-dimethylpyridin-3-yl)-2-oxoacetate (1.9 g, 5.63 mmol) at rt. The resulting mixture was placed in a pre-heated oil bath (80 C) and stirred for 18 h; cooled, and concentrated. The crude product was charged (DCM) to a 80 g ISCO silica gel cartridge and gradient elution (5 – 35% EtOAc/hexanes) using an Isolera chromatography station to give isopropyl 2-(5-bromo-2,6-dimethyl-4-(2-oxa-8-azaspiro[4.5]decan-8-yl)pyridin-3- yl)-2-oxoacetate 990 mg (40%). 1H NMR (500 MHz, CDC13) delta 5.08-5.05 (m, 1H), 3.75 (t, J=7.3 Hz, 2H), 3.37 (s, 2H), 3.36-3.34 (m, 4H), 2.61 (s, 3H), 2.30 (s, 3H), 1.73-1.71 (m, 2H), 1.50 (br. s, 4H), 1.29 (d, J=6.2 Hz, 6H). UPLC (M+H) = 441.1.

479195-19-2, 479195-19-2 2-Oxa-8-azaspiro[4.5]decane hydrochloride 21955264, apiperidines compound, is more and more widely used in various fields.

Reference£º
Patent; VIIV HEALTHCARE UK (NO.5) LIMITED; KADOW, John F.; NAIDU, B. Narasimhulu; ROMINE, Jeffrey Lee; SIVAPRAKASAM, Prasanna; ST. LAURENT, Denis R.; (204 pag.)WO2017/25864; (2017); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem