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ChemicalBook CAS DataBase List Thieno[3,2-d]pyrimidine-7-carboxylic acid, 4-chloro-

Thieno[3,2-d]pyrimidine-7-carboxylic acid, 4-chloro- synthesis

10synthesis methods
-

Yield: 81%

Reaction Conditions:

with lithium hydroxide monohydrate;water in tetrahydrofuran at 20; for 2 h;

Steps:

8.A
To a solution of methyl 4-chlorothieno[3,2-d]pyrimidine-7-carboxylate (2.00 g, 8.75 mmol) in tetrahydrofuran (60 mL) and water (20 mL) was added lithium hydroxide monohydrate (0.59 g, 14.0 mmol). The reaction mixture was stirred at room temperature for 2 hours, after which the volatiles were concentrated in vacuo. Water was added and a solid was obtain after filtration, which was rinsed with water and dried on a lyophilizer to afford 4-chlorothieno[3,2-fiT]pyrimidine-7-carboxylic acid (1.56 g, 81%).

References:

ARRAY BIOPHARMA INC.;GENENTECH, INC.;ALIAGAS, Ignacio;GRADL, Stefan;GUNZNER, Janet;MATHIEU, Simon;PULK, Rebecca;RUDOLPH, Joachim;WEN, Zhaoyang;GRINA, Jonas;HANSEN, Joshua D.;LAIRD, Ellen;MORENO, David;REN, Li;WENGLOWSKY, Steven Mark WO2011/25940, 2011, A1 Location in patent:Page/Page column 96