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HRID 1428844作成日:2026年10月26日

Potassium Carbonate → 1-[6-cyclopropyl-4-oxo-3-(2-trimethylsilanylethoxymethyl)-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1428844

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Cyclopropylboronic acidHCID 2760897—
反応物1-[6-bromo-4-oxo-3-(2-trimethylsilanyl-ethoxymethyl)-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl esterHCID 68488554—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 44119782—
溶媒TetrahydrofuranHCID 8028—
生成物1-[6-cyclopropyl-4-oxo-3-(2-trimethylsilanylethoxymethyl)-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6848687226.1%

反応条件

温度80 °C

反応手順

A mixture of 1-[6-bromo-4-oxo-3-(2-trimethylsilanyl-ethoxymethyl)-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester (0.500 g, 1.01 mmol), cyclopropylboronic acid (0.199 g, 2.32 mmol), dichloro(1,1′-bis(diphenylphosphino)ferrocene)palladium(II)dichloromethane adduct (0.100 g, 0.123 mmol), K2CO3 (0.420 g, 3.04 mmol) and THF (10 mL) were purged for 15 minutes with nitrogen and then heated to 80° C. for 15 h. The mixture was cooled to room temperature and filtered through a pad of CELITE®. The filtrate cake was washed with dichloromethane and concentrated. The residue was purified by FCC (0-20% EtOAc/hexanes) to yield the titled compound (0.120 g, 26% yield). MS (ESI/Cl): mass calcd. for C23H30N4O4Si, 454.2; m/z found, 455.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08937078B2
出典データセットuspto-grants-2015_01
ORD IDord-c02a841d37c440aea8bc450ac28c5840
出典メモuspto-grants-2015_01