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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266273생성일: 2026년 10월 26일

3,4-dihydro-2H-pyran → (RS)-2-(4-chlorobenzenesulfonylamino)-N-(5-methoxycarbonylpentyl)-3-(tetrahydropyran-2-yloxy)propanamide

https://huagongshe.com/reaction/266273

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물2-(4-Chlorobenzenesulfonamido)-3-hydroxypropanoic acidHCID 4229170—
반응물Methyl 6-aminohexanoate hydrochlorideHCID 11499324—
생성물(RS)-2-(4-chlorobenzenesulfonylamino)-N-(5-methoxycarbonylpentyl)-3-(tetrahydropyran-2-yloxy)propanamideHCID 19032787—

반응 단계

The procedure described in Example 1 was repeated, except that dihydropyran (2.56 ml) and methyl 6-aminohexanate hydrochloride (3.41 g) were successively reacted with (RS)-2-(4-chlorobenzenesulfonylamino)-3-hydroxypropanoic acid (4.94 g) to obtain (RS)-2-(4-chlorobenzenesulfonylamino)-N-(5-methoxycarbonylpentyl)-3-(tetrahydropyran-2-yloxy)propanamide (0.87 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650428
출처 데이터셋uspto-grants-1997_07
ORD IDord-6b3e2282d0434f81a4d515c4b4627bca
출처 메모uspto-grants-1997_07