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HRID 1853441作成日:2026年10月26日

p-Toluenesulfonic acid → 4-Methyl-2-ethylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1853441

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Ethyl AcetoacetateHCID 8868—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物S-Ethylisothiuronium bromideHCID 200213—
溶媒DimethylformamideHCID 6228—
生成物4-Methyl-2-ethylsulfanyl-pyrimidine-5-carboxylic acid ethyl esterHCID 6843665162.7%

反応条件

温度100 °C

反応手順

A mixture of ethyl acetoacetate (6.37 mL, 50.0 mol), dimethylformamide dimethylacetal (8.94 g, 75.0 mmol), and catalytic p-toluenesulfonic acid was heated at 100° C. for 2 h. After cooling to rt, the mixture was diluted with N,N-dimethylformamide (DMF; 50 mL) and 2-ethylisothiourea hydrobromide (9.10 g, 50.0 mmol) was added. After heating the at 100° C. for 18 h, the mixture was cooled to rt and concentrated to give a crude residue, which was purified by FCC (EtOAc/hexanes) to give 7.1 g (61%) of a solid. 1H NMR (CDCl3): 8.97-8.91 (m, 1H), 4.43-4.35 (m, 2H), 3.24-3.15 (m, 2H), 2.81-2.72 (m, 3H), 1.47-1.35 (m, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08962644B2
出典データセットuspto-grants-2015_02
ORD IDord-4a97bec3cc0c435d9193e78165c0e87a
出典メモuspto-grants-2015_02