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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32056생성일: 2026년 10월 23일

Isopropylamine → N-[7-(isopropylamino-methyl)-chroman-4-yl]-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide

https://huagongshe.com/ko/reaction/32056

반응식

참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물DiisopropylethylamineHCID 81531—
반응물Methanesulfonic anhydrideHCID 81560—
반응물N-(7-hydroxymethyl-chroman-4-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamideHCID 68932544—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물N-[7-(isopropylamino-methyl)-chroman-4-yl]-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamideHCID 68928313—

반응 조건

온도0 °C

반응 단계

N-(7-Hydroxymethyl-chroman-4-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide (Step A) (0.050 g, 0.010 mmol) and DIEA (0.038 g, 0.030 mmol) were dissolved in THF (1.5 mL). The solution was cooled to 0° C. and methanesulfonic anhydride (0.023 g, 0.014 mmol) was added. After the reaction was stirred for 3.5 h, isopropylamine (0.14 g, 2.3 mmol) was added and the solution was stirred at RT overnight. The reaction was diluted with CHCl3 and washed with brine. The aqueous phase was extracted once with CHCl3. The organic phases were combined, dried over MgSO4, filtered, and concentrated in vacuo to provide a residue which was purified by column chromatography (silica, 0.2% TEA in acetone) to provide the title compound. MS (ESI) m/z 558 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425631B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5e3421b9ffec4c83ab2a6feeab9ea2e4
출처 메모uspto-grants-2008_09