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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501955생성일: 2026년 10월 24일

Lithium hydroxide, monohydrate → (R)-3-(7-Methyl-1H-indazol-5-yl)-2-(4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)propanoic acid

https://huagongshe.com/ko/reaction/501955

반응식

참여 물질

역할이름HCID투입량
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물(R)-1-Methoxy-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylateHCID 59424336—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(R)-3-(7-Methyl-1H-indazol-5-yl)-2-(4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)propanoic acidHCID 59424312—

반응 조건

온도0 °C

반응 단계

To a solution of (R)-1-methoxy-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate (1.20 g, 2.46 mmol) in methanol (10 mL) and tetrahydrofuran (10 mL) at 0° C. was added a precooled solution of lithium hydroxide monohydrate (309 mg, 3.0 equiv) in water (10 mL). After 2 h, the reaction was concentrated under high vaccuum (<25° C.). The resulting residue was dissolved in water (20 mL), cooled to 0° C., and acidified to ca. pH 2 with 1 N hydrochloric acid. The suspension was maintained at 0° C. for 1 h, filtered, and the solid washed with cold water. The resulting white solid was air dried and then dried under high vacuum overnight to give 1.04 g (89%) as a white solid. Mass spec.: 475.30 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772244B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-fc096ab435514d8d89557808b6c67626
출처 메모uspto-grants-2010_08