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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803078생성일: 2026년 10월 26일

Diisopropylethylamine → 1-Methyl-piperidine-4-carboxylic acid [2-(2-methoxy-benzylamino)-quinolin-6-yl]-amide

https://huagongshe.com/reaction/1803078

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물4-Piperidinecarboxylic acid, 1-methyl-, hydrochloride (1:1)HCID 2760043—
반응물N2-(2-Methoxy-benzyl)-quinoline-2,6-diamineHCID 43450845—
용매TetrahydrofuranHCID 8028—
생성물1-Methyl-piperidine-4-carboxylic acid [2-(2-methoxy-benzylamino)-quinolin-6-yl]-amideHCID 8663442148.3%

반응 단계

To a stirred solution of 1-methyl-piperidine-4-carboxylic acid hydrochloride salt (35 mg, 179 mmol) in tetrahydrofurane (3 ml) were added at room temperature N-ethyldiisopropylamine (74 mg, 0.573 mmol), 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (27 mg, 0.197 mmol), N,N-diisopropyl ethyl amine (74 mg, 0.197 mmol) and 1-(3-dimethylamino-propyl)-3-ethylcarbodiimide hydrochloride (38 mg, 0.197 mmol) and the mixture was allowed to stir for 90 min. N2-(2-Methoxy-benzyl)-quinoline-2,6-diamine (example 10, step B, 50 mg, 0.179 mmol) was added and the reaction mixture was allowed to stir for 17 h, poured into sat. sodium bicarbonate solution (30 ml) and extracted with dichloromethane (2×30 ml). The combined organic layers were washed with water (30 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (heptane/ethyl acetate) and crystallization (ethyl acetate/heptane) to yield the title compound as white solid (35 mg, 48%). MS: m/e=405.5 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08350028B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-4d48e4bd7fbe4e64b5a0cbe33b7701ed
출처 메모uspto-grants-2013_01