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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1159677생성일: 2026년 10월 27일

2-Naphthoic acid → Methyl {4-methyl-2-[4-(2-naphthoylamino)benzyl]-6-pyrrolidin-1-ylpyrimidin-5-yl}acetate

https://huagongshe.com/reaction/1159677

반응식

참여 물질

역할이름HCID투입량
반응물2-Naphthoic acidHCID 7123—
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물Methyl[2-(4-aminobenzyl)-4-methyl-6-pyrrolidin-1-ylpyrimidin-5-yl]acetateHCID 59514524—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Methyl {4-methyl-2-[4-(2-naphthoylamino)benzyl]-6-pyrrolidin-1-ylpyrimidin-5-yl}acetateHCID 5951453936.4%

반응 단계

A solution of methyl [2-(4-aminobenzyl)-4-methyl-6-pyrrolidin-1-ylpyrimidin-5-yl]acetate (0.034 g, 0.10 mmol) in THF (1 mL) at room temperature was treated with PyBOP (0.052 g, 0.10 mmol), 2-naphthoic acid (0.019 g, 0.11 mmol), and N,N-diisopropylethylamine (0.017 mL, 0.10 mmol). After stirring at room temperature for 17 hours, the reaction mixture was poured into water and extracted with EtOAc. The combined organic extracts was dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The remaining residue was chromatographed over silica gel eluting with 60% EtOAc in CH2Cl2 to give methyl {4-methyl-2-[4-(2-naphthoylamino)benzyl]-6-pyrrolidin-1-ylpyrimidin-5-yl}acetate (0.018 g, 36% yield) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07812160B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-b6b6eba1e82e4ca1ae85f92f6d74c31a
출처 메모uspto-grants-2010_10