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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2070724생성일: 2026년 10월 25일

Cyclopropylamine → N-Cyclopropyl-4-methyl-3-[3-[[[2-(methylthio)phenyl]methyl]amino]-2-oxo-1(2H)-pyrazinyl]-benzamide

https://huagongshe.com/reaction/2070724

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropylamineHCID 69828—
반응물2-(Methylthio)benzylamineHCID 2736981—
반응물4-Methyl-3-(2-oxo-3-phenoxy-1(2H)-pyrazinyl)-benzoic acid, methyl esterHCID 86663239—
반응물HCID 178419650HCID 178419650—
용매TetrahydrofuranHCID 8028—
생성물N-Cyclopropyl-4-methyl-3-[3-[[[2-(methylthio)phenyl]methyl]amino]-2-oxo-1(2H)-pyrazinyl]-benzamideHCID 66686300—

반응 조건

온도120 °C

반응 단계

A mixture of 4-methyl-3-(2-oxo-3-phenoxy-2H-pyrazin-1-yl)-benzoic acid, methyl ester (Example 128a, 111 mg), 2-(methylthio)-benzenemethanamine (100 mg) and tetrahydrofuran (1 mL) was heated within a microwave for 5 h at 120° C. before being cooled to room temperature. Cyclopropylamine (0.2 mL) was added followed by addition of cyclopentylmagnesium bromide (2M in diethyl ether, 0.8 mL). The mixture was stirred for 10 min., quenched with sat. NH4Cl and extracted into ethyl acetate. The organic phase was concentrated in vacuo. Purification by preparative HPLC (Gemini column, 0.1% ammonia: acetonitrile eluent) afforded the title compound as a solid (39 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08299246B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-41bb6d6a6c0b46079d3b58f17f9a098f
출처 메모uspto-grants-2012_10