Triethylamine → methyl 2-(6-ethyl-2,4-dioxo-1,4-dihydrothieno[2,3-d]pyrimidin-3(2H)-yl)propanoate

To a solution (500 mL) of methyl 2-amino-5-ethylthiophene-3-carboxylate (15 g) in methylene chloride were added triphosgene (10.4 g) and triethylamine (29.4 mL), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture were further added triethylamine (24.8 mL) and DL-alanine methyl ester hydrochloride (22.6 g), and the mixture was further stirred at room temperature for 1 hr, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in methanol (500 mL), sodium methoxide (21.9 g) was added, and the mixture was stirred at 60° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was extracted with 1N hydrochloric acid and chloroform. The chloroform layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as a colorless solid (9.96 g, 44%).

1. stirringthe mixture was further stirred at room temperature for 1 hr
2. washwashed with water and saturated brine
3. dry with materialdried over anhydrous magnesium sulfate
4. customThe solvent was evaporated under reduced pressure
5. dissolutionThe obtained residue was dissolved in methanol (500 mL)
6. additionsodium methoxide (21.9 g) was added
7. stirringthe mixture was stirred at 60° C. for 1 hr
8. concentrationThe reaction mixture was concentrated under reduced pressure
9. extractionthe obtained residue was extracted with 1N hydrochloric acid and chloroform
10. washThe chloroform layer was washed with saturated brine
11. dry with materialdried over anhydrous magnesium sulfate
12. customThe solvent was evaporated under reduced pressure
13. filtrationThe precipitated solid was collected by filtration

ORD-Eintrag

ord-50efb30bf7dd4376a826ce845466cf03

Quelldatensatz

uspto-grants-2013_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08501750B2