Diethyl (ethoxymethylene)malonate → Ethyl 1,6-dihydro-1-(2-methoxyethyl)-6-oxo-2-(3-thienyl)-5-pyrimidinecarboxylate

2-Methoxy-1-ethylamine (0.86 g, 11.4 mmol) was added to a solution of 3-thiophenecarboximidic acid ethyl ester hydrochloride (2.0 g, 10.4 mmol) in methanol (10 mL), which was then stirred at ambient temperature for 1.5 h. The reaction mixture was then concentrated under reduced pressure and redissolved in ethanol (10 mL). Sodium ethoxide solution (21% w/w in ethanol, 3.4 g, 10 mmol) and diethyl ethoxymethylenemalonate (2.2 g, 10 mmol) were added and the mixture was heated to reflux for 2 h before being concentrated under reduced pressure and purified by medium pressure liquid chromatography on silica gel eluting with 0 to 100% ethyl acetate in hexanes to provide 1.82 g of the title compound as an oil.

1. concentrationThe reaction mixture was then concentrated under reduced pressure
2. dissolutionredissolved in ethanol (10 mL)
3. temperaturethe mixture was heated
4. temperatureto reflux for 2 h
5. concentrationbefore being concentrated under reduced pressure
6. custompurified by medium pressure liquid chromatography on silica gel eluting with 0 to 100% ethyl acetate in hexanes

ORDレコード

ord-7834bbf3631448ec96a6258f1b6ce942

出典データセット

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09187432B2