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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32918생성일: 2026년 10월 24일

Dimethylformamide → 1-(2-Trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carboxylic acid (2-piperidin-1-yl-phenyl)-amide

https://huagongshe.com/ko/reaction/32918

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물2-(Piperidin-1-yl)anilineHCID 458795—
반응물1-(2-Trimethylsilanyl-ethoxymethyl)-1h-imidazole-4-carboxylate sodium saltHCID 68682339—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매Ethyl AcetateHCID 8857—
생성물1-(2-Trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carboxylic acid (2-piperidin-1-yl-phenyl)-amideHCID 5979465199.9%

반응 단계

A flask was charged with 1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carboxylate sodium salt (70 mg, 0.26 mmol) (as prepared in the previous step), 2-piperidin-1-yl-phenylamine (36 mg, 0.20 mmol), EDCI (60 g, 0.31 mmol), DMAP (25 mg, 0.20 mmol), and DMF (1 mL) and stirred for 3 h at RT. The reaction was diluted with EtOAc (10 mL) and washed with brine (2×10 mL), and the organic layer was dried over Na2SO4 and then concentrated. The title compound was eluted from a 5-g SPE cartridge (silica) with 30% EtOAc/hexane to give 80 mg (97%) of a white solid. Mass spectrum (ESI, m/z): Calcd. for C21H32N4O2Si, 401.2 (M+H), found 401.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427683B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ff6beeb2e0844a1bb1d7837d454fcc2e
출처 메모uspto-grants-2008_09