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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2110060생성일: 2026년 10월 27일

Tributylphosphine → 6-Chloro-N-(3-furylmethyl)-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide

https://huagongshe.com/reaction/2110060

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물3-FuranmethanolHCID 20449—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-(4-morpholinyl)-2-oxo ethyl]-2-oxo-3-pyrrolidinyl}-2-naphthalenesulfonamideHCID 6852168—
용매TetrahydrofuranHCID 8028—
생성물6-Chloro-N-(3-furylmethyl)-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamideHCID 10143807—

반응 단계

A solution of 6-chloro-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide [Example 1] (0.015 g) in THF (0.5 ml) was treated with diisopropyl azodicarboxylate (0.01 ml), 3-furanmethanol (0.004 ml) and tri-n-butylphosphine (0.008 ml) and shaken at room temperature for 60 h. The mixture was concentrated under reduced pressure and the residue purified by mass directed preparative h.p.l.c. to give the title compound (0.015 g) as a colourless gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517879B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-46aaf0c937604416b2c99c08c19ab451
출처 메모uspto-grants-2009_04