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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1765651생성일: 2026년 10월 26일

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/reaction/1765651

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 번호US07226929B2
출처 데이터셋uspto-grants-2007_06
ORD IDord-230001f9c194409d85894f0beb6fdf21
출처 메모uspto-grants-2007_06