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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7317생성일: 2026년 10월 23일

Acetic Acid → 6-Chloro-N-((3S)-1-{(1S)-2-[3-(ethylamino)piperidin-1-yl]-1-methyl-2-oxoethyl}-2-oxopyrrolidin-3-yl)naphthalene-2-sulfonamide

https://huagongshe.com/ko/reaction/7317

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AcetaldehydeHCID 177—
반응물N-((3S)-1-[(1S)-2-(3-aminopiperidin-1-yl)-1-methyl-2-oxoethyl]-2-oxopyrrolidin-3-yl)-6-chloronaphthalene-2-sulfonamideHCID 69329851—
반응물Tetraethylammonium triacetoxyborohydrideHCID 131725882—
용매DichloromethaneHCID 6344—
생성물6-Chloro-N-((3S)-1-{(1S)-2-[3-(ethylamino)piperidin-1-yl]-1-methyl-2-oxoethyl}-2-oxopyrrolidin-3-yl)naphthalene-2-sulfonamideHCID 69329588—

반응 단계

To a solution of acetaldehyde (0.041 ml from a stock solution made up from 0.0127 l acetaldehyde dissolved in 1 ml DCM)) in dry DCM (0.4 ml) treated with acetic acid (0.1 ml from a stock solution made up from 0.0054 ml acetic acid dissolved in 1 ml DCM) was added N-{(3S)-1-[(1S)-2-(3-aminopiperidin-1-yl)-1-methyl-2-oxoethyl]-2-oxopyrrolidin-3-yl }-6-chloronaphthalene-2-sulfonamide [Example 365] (0.045 g) followed by tetraethylammonium triacetoxyborohydride (0.005 g). The mixture was stirred at room temperature, under nitrogen, for 60 h. DCM (1 ml) was added and the resultant solution washed with saturated sodium bicarbonate (1 ml) in a hydrophobic frit. The solvent was concentrated under reduced pressure and the residue purified by mass directed preparative h.p.l.c. to give the title compound (0.8 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084139B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-993085dca3ef4537b2715ac868b3332c
출처 메모uspto-grants-2006_08