Category: 79836-78-5

More research is needed about 79836-78-5

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C7H9NO2S. In my other articles, you can also check out more blogs about 79836-78-5

79836-78-5, Name is Ethyl 2-methylthiazole-5-carboxylate, molecular formula is C7H9NO2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 79836-78-5, HPLC of Formula: C7H9NO2S

The present invention relates to a novel family of inhibitors of protein kinases. In particular, the present invention relates to inhibitors o f the members o f the Tec and Src protein kinase families

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C7H9NO2S. In my other articles, you can also check out more blogs about 79836-78-5

Reference£º
Thiazole | C3H8171NS – PubChem,
Thiazole | chemical compound | Britannica

Brief introduction of 79836-78-5

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: Ethyl 2-methylthiazole-5-carboxylate. In my other articles, you can also check out more blogs about 79836-78-5

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 79836-78-5, Name is Ethyl 2-methylthiazole-5-carboxylate, molecular formula is C7H9NO2S. In a Patent£¬once mentioned of 79836-78-5, name: Ethyl 2-methylthiazole-5-carboxylate

The invention relates to crystalline tripeptide keto epoxide compounds, methods of their preparation, and related pharmaceutical compositions

The invention relates to crystalline tripeptide keto epoxide compounds, methods of their preparation, and related pharmaceutical compositions

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: Ethyl 2-methylthiazole-5-carboxylate. In my other articles, you can also check out more blogs about 79836-78-5

Reference£º
Thiazole | C3H8178NS – PubChem,
Thiazole | chemical compound | Britannica

New learning discoveries about 79836-78-5

The synthetic route of 79836-78-5 has been constantly updated, and we look forward to future research findings.

79836-78-5, Ethyl 2-methylthiazole-5-carboxylate is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Step 1: Intermediate 15-a To a solution of ethyl 2-methylthiazole-5-carboxylate (5.82 g, 34.0 mmol) in THF (170 ml), cooled to 0 C, was added a 1.0M solution of LiAIH4 in THF (34.0 ml, 34.0 mmol) and the reaction was slowly warmed to room temperature and stirred overnight. Water (1.3 ml) was slowly added, followed by 15% NaOH (1.3 ml_). The solution was stirred for 2 hours at room temperature then filtered over celite. The filtrate was concentrated under reduced pressure to provide intermediate 15-a as a yellow oil., 79836-78-5

The synthetic route of 79836-78-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; PHARMASCIENCE, INC.; LAURENT, Alain; ROSE, Yannick; JAQUITH, James B.; WO2013/177668; (2013); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

Analyzing the synthesis route of 79836-78-5

The synthetic route of 79836-78-5 has been constantly updated, and we look forward to future research findings.

79836-78-5,79836-78-5, Ethyl 2-methylthiazole-5-carboxylate is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

To a 0¡ã C. solution of ethyl 2-methyl-thiazole-5-carboxylate (15 g, 88 mmol) in tetrahydrofuran (50 mL) was added aqueous sodium hydroxide solution (5 N, 50 mL) over 10 minutes, and the resulting solution was stirred at room temperature for another 2 hours. It was then acidified with hydrochloric acid (2 N) to pH=1 and extracted with tetrahydrofuran (3¡Á100 mL). The combined organic layers were washed with brine (30 mL) and dried over sodium sulfate. Most of the solvents were removed under reduced pressure and the residue was lyophilized to afford Compound (E) (14 g).

The synthetic route of 79836-78-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; AMGEN INC.; CHUNG, John Inn; PIRJANIAN, Armen; ALVAREZ-NUNEZ, Fernando Antonio; KATZ, Jeffrey Michael; DAURIO, Dominick Paul; LA, Stevedat; KENNEDY, Michael T.; (52 pag.)US2018/161279; (2018); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica

Downstream synthetic route of 79836-78-5

The synthetic route of 79836-78-5 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.79836-78-5,Ethyl 2-methylthiazole-5-carboxylate,as a common compound, the synthetic route is as follows.

To a stirred solution of ethyl 2-methylthiazole-5-carboxylate (1 eq) in dry THF (5 mL) at 0 Patent; MERCK PATENT GMBH; YU, Henry; LIU-BUJALSKI, Lesley; JOHNSON, Theresa L.; WO2014/159234; (2014); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica