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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7301생성일: 2026년 10월 24일

3-Methylpiperidine → 6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-(3-methylpiperidin-1-yl)-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide

https://huagongshe.com/ko/reaction/7301

반응식

참여 물질

역할이름HCID투입량
반응물3-MethylpiperidineHCID 79081—
반응물(2S)-2-((3S)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acidHCID 69058818—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매DiisopropylethylamineHCID 81531—
생성물6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-(3-methylpiperidin-1-yl)-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamideHCID 6932959627.3%

반응 단계

To polymer N-cyclohexylcarbodiimide-N′-propyloxymethyl polystyrene (0.038 g) in an Alltech™ tube was added a solution of (2S)-2-((3S)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid (0.007 g) in DCM (0.9 ml) followed by 3-methylpiperidine (0.0025 g) in DMF (0.1 ml) and N,N-diisopropylethylamine (0.006 ml). The mixture was shaken at room temperature for 4 days. The tube was drained, the filtrate collected and the resin washed with DCM. The combined DCM solutions were concentrated under reduced pressure and the residue purified by mass directed preparative h.p.l.c. to give the title compound (0.0023 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084139B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3cee8656047a4293930211c443eeb1e4
출처 메모uspto-grants-2006_08