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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80826생성일: 2026년 10월 23일

4-Pyrrolidinopyridine → 1-(2-chloro-4-methyl-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)-3-cyclopropylpropane-1,3-dione

https://huagongshe.com/ko/reaction/80826

반응식

참여 물질

역할이름HCID투입량
반응물4-PyrrolidinopyridineHCID 75567—
반응물DiisopropylethylamineHCID 81531—
반응물3-Cyclopropyl-3-Oxopropionic Acid Methyl EsterHCID 10130016—
반응물2-Chloro-4-methyl-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochlorideHCID 86690268—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물1-(2-chloro-4-methyl-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)-3-cyclopropylpropane-1,3-dioneHCID 8669027552.4%

반응 단계

Microwave was used to irradiated a suspension of 2-chloro-4-methyl-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride (1.00 g, 4.56 mmol), methyl 3-cyclopropyl-3-oxopropanoate (1.298 g, 9.13 mmol), 4-pyrrolidinopyridine (0.068 g, 0.456 mmol) and DIPEA (1.20 mL, 6.85 mmol) in toluene (10 mL) at 150° C. for 45 min. The mixture was cooled to rt and diluted with 1 M HClaq (10 mL) and EtOAc. The products were extracted twice with EtOAc. The combined organic layer was washed with a mixed solution of 1M HClaq/brine (1 mL/2 mL), dried over Na2SO4, filtered, and concentrated to give crude. The residue was purified by flash column chromatography on 12 g of silica gel (eluent: DCM/EtOAc=90:10 to 0:100) to give crude 1-(2-chloro-4-methyl-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)-3-cyclopropylpropane-1,3-dione (0.70 g): MS (ESI+) m/z 293.31 (M+H)+. The obtained material was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846656B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2d46bcc181424193a06a8e1009f26c20
출처 메모uspto-grants-2014_09