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HRID 459906作成日:2026年10月25日

Ethyl ethoxyacetate → 2-Butylsulfanyl-6-ethoxy-8,8a-dihydro-4ahpyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/459906

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl ethoxyacetateHCID 69955—
反応物HCID 21956055HCID 21956055—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TolueneHCID 1140—
生成物2-Butylsulfanyl-6-ethoxy-8,8a-dihydro-4ahpyrido[2,3-d]pyrimidin-7-oneHCID 21956051—

反応手順

4-Amino-2-butylsulfanyl-4,5-dihydro-pyrimidine-5-carbaldehyde (3 g, 14.2 mmol, furnished by scaleup) and ethyl ethoxyacetate (2.34 g, 2.4 ml, 17.75 mmol) were stirred in 80 ml toluene at 0°-5° C. under nitrogen. Potassium t-butoxide (1.75 g, 15.6 mmol) was added gradually. The mixture was stirred to ambient temperature, and then to 65° C. for 48 hours. An additional 20 ml of toluene and 2.4 ml ethyl ethoxyacetate were added and the reaction was maintained at 65° C. over the weekend. The reaction mixture was concentrated in vacuo and triturated with EtOAc to remove the remaining starting aldehyde. The remaining solid was further triturated with chloroform to remove additional impurities. 3.66 g of 2-Butylsulfanyl-6-ethoxy-8,8a-dihydro-4aHpyrido[2,3-d]pyrimidin-7-one (1A) of a purity greater than 80% as judged by MS/HPLC and NMR was collected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196097B2
出典データセットuspto-grants-2007_03
ORD IDord-6cd10b64cb5b47d8a8a9f9930b4e7750
出典メモuspto-grants-2007_03