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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29090생성일: 2026년 10월 23일

Ethyl Acetate → Methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate

https://huagongshe.com/ko/reaction/29090

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물3,5-DimethylpyridineHCID 11565—
반응물Methanesulfonic anhydrideHCID 81560—
반응물Methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylateHCID 11232707—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물Methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylateHCID 1140710286.1%

반응 단계

A solution of (MeSO2)2O (15.9 g, 0.091 mol) in anhydrous CH2Cl2 (50 mL) was added to a solution of Part C methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate (10. g, 0.030 mol) and 3,5-lutidine (20.9 mL, 0.182 mol) in anhydrous toluene (100 mL) at room temperature. The reaction mixture was stirred at room temperature for 3 days. Ethyl acetate (200 mL) and H2O (50 mL) were added, and the resulting two phases were separated. The organic phase was washed with aqueous NaHCO3 (5%, 50 mL), followed by half-saturated brine (50 mL). The solvent was removed under reduced pressure to afford a yellowish oil which solidified slowly. The crude material was recrystallized from i-PrOH/H2O (85:15, 45 mL) to afford 10.5 g (85% yield) of methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate as a off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420059B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f1e16f2f645848c08392fcd476819a3b
출처 메모uspto-grants-2008_09