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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1765667생성일: 2026년 10월 26일

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/reaction/1765667

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 0.01271 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 (0.0059 ). 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 번호US07226929B2
출처 데이터셋uspto-grants-2007_06
ORD IDord-667c5f55cc8e4b4f8b64e011fe6d6a7b
출처 메모uspto-grants-2007_06