Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 337044생성일: 2026년 10월 24일
Cyclopropylamine → N-Cyclopropyl-4-methyl-3-[3-[[[2-(methylthio)phenyl]methyl]amino]-2-oxo-1(2H)-pyrazinyl]-benzamide
https://huagongshe.com/ko/reaction/337044
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclopropylamine | HCID 69828 | — |
| 반응물 | 2-(Methylthio)benzylamine | HCID 2736981 | — |
| 반응물 | 4-Methyl-3-(2-oxo-3-phenoxy-1(2H)-pyrazinyl)-benzoic acid, methyl ester | HCID 86663239 | — |
| 반응물 | HCID 178419650 | HCID 178419650 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Cyclopropyl-4-methyl-3-[3-[[[2-(methylthio)phenyl]methyl]amino]-2-oxo-1(2H)-pyrazinyl]-benzamide | HCID 66686300 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08889692B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_11 |
|---|
| ORD ID | ord-c25f112a054e4f8a8e90ad4b9bef77e6 |
|---|
| 출처 메모 | uspto-grants-2014_11 |
|---|