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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1504181생성일: 2026년 10월 26일

1-Hydroxybenzotriazole → 2,3-Dihydrobenzofuran-7-carboxylic acid methyl-(2-{[3-(1-methyl-2-oxo-1,2-dihydroquinolin-6-yloxy)propyl]pyridin-4-ylmethylamino}ethyl)amide dihydrochloride

https://huagongshe.com/reaction/1504181

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물CarbodiimideHCID 160435—
반응물2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 2795014—
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
반응물1-Methyl-6-{3-[(2-methylamino-ethyl)-pyridin-4-ylmethyl-amino]-propoxy}-1H-quinolin-2-oneHCID 66960579—
용매AcetonitrileHCID 6342—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2,3-Dihydrobenzofuran-7-carboxylic acid methyl-(2-{[3-(1-methyl-2-oxo-1,2-dihydroquinolin-6-yloxy)propyl]pyridin-4-ylmethylamino}ethyl)amide dihydrochlorideHCID 70657180—

반응 단계

PS-Carbodiimide resin(1.3 g) and 1-hydroxy benzotriazole (HOBt) (230 mg) were added to acetonitrile and THF solution (4 ml+6 ml) of 1-methyl-6-{3-[(2-methylamino ethyl)pyridin-4-ylmethylamino]propoxy}-1H-quinolin-2-one(304 mg) and 2,3-dihydrobenzofuran-7-carboxylic acid(164 mg). The mixture was stirred at room temperature overnight. After the reaction mixture was filtrated and condensed under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate: methanol=1:0→10:1). The purified product was condensed under reduced pressure. A 4N-hydrogen chloride ethyl acetate solution(0.35 ml) was added to an ethyl acetate solution of the residue. The precipitated insoluble matter was separated, washed with ethyl acetate, and dried to give the title compound(324.2 mg) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09212187B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-9158af4bec874db3957a1078403b2886
출처 메모uspto-grants-2015_12