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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362127생성일: 2026년 10월 27일

Tri-o-tolylphosphine → (E)-N-(1H-indol-3-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamide

https://huagongshe.com/reaction/1362127

반응식

참여 물질

역할이름HCID투입량
반응물Tri-o-tolylphosphineHCID 80271—
반응물DiisopropylethylamineHCID 81531—
반응물6-Bromo-3,4-dihydro-1,8-naphthyridin-2(1H)-oneHCID 11096325—
반응물N-(1H-indol-3-ylmethyl)-N-methylacrylamideHCID 22139147—
촉매palladium(II) acetateHCID 167845—
용매PropionitrileHCID 7854—
생성물(E)-N-(1H-indol-3-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamideHCID 1031647637%

반응 단계

A solution of 6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one (0.64 g, 2.80 mmole), N-(1H-indol-3-ylmethyl)-N-methylacrylamide (0.60 g, 2.80 mmole), Pd(OAc)2 (0.06 g, 0.28 mmole), tri-ortho-tolylphosphine (0.17 g, 0.56 mmole) and diisopropylethylamine (0.73 mL, 4.2 mmole) in propionitrile (50 mL) was deoxygenated, then was heated to reflux under N2 overnight. The dark mixture was filtered through a pad of Celite®, and the filter pad was rinsed with acetonitrile (250 mL). The filtrate was concentrated in vacuo, and the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3). The title compound (0.37 g, 37%) was obtained as a light yellow solid after drying in vacuo: MS (ES) m/e 361 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-7d282b7441a34081b7cc7e5d6aae21ab
출처 메모uspto-grants-2011_02