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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266272생성일: 2026년 10월 25일

3,4-dihydro-2H-pyran → (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-methoxycarbonylbutyl)-3-(tetrahydropyran-2-yloxy)propanamide

https://huagongshe.com/reaction/266272

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물2-(4-Chlorobenzenesulfonamido)-3-hydroxypropanoic acidHCID 4229170—
반응물Methyl 5-aminopentanoate hydrochlorideHCID 13672034—
생성물(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-methoxycarbonylbutyl)-3-(tetrahydropyran-2-yloxy)propanamideHCID 19032845—

반응 단계

The procedure described in Example 1 was repeated, except that dihydropyran (2.9 ml) and methyl 5-aminopentanate hydrochloride (2.158 g) were successively reacted with (RS)-2-(4-chlorobenzenesulfonylamino)-3-hydroxypropanoic acid (3 g) to obtain (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-methoxycarbonylbutyl)-3-(tetrahydropyran-2-yloxy)propanamide (2.059 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650428
출처 데이터셋uspto-grants-1997_07
ORD IDord-30447eeba407456a81c808bac96e9da9
출처 메모uspto-grants-1997_07