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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388568생성일: 2026년 10월 25일

Triethylamine → 1-Piperidinecarboxylic acid, ethyl ester

https://huagongshe.com/reaction/388568

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물HCID 24816438HCID 24816438—
용매DimethylformamideHCID 6228—
생성물1-Piperidinecarboxylic acid, ethyl esterHCID 21399—

반응 단계

To a mixture of 6-{5-Chloro-4-[2-(propane-2-sulfonyl)-phenylamino]-pyrimidin-2-ylamino}-5-isopropoxy-2-piperidin-4-yl-2,3-dihydro-isoindol-1-one (Example 1, 15 mg, 0.025 mmol) and triethylamine (37.5 uL, 0.25 mmol) in DMF (0.5 mL), is added ethyl chloroformate (5.4 mg, 0.05 mmol). The mixture is stirred at room temperature for 1 hour. The crude reaction mixture is purified by mass-trigger preparative RP LC-MS to afford the title compound 446-{5-chloro-4-[2-(propane-2-sulfonyl)-phenylamino]-pyrimidin-2-ylamino}-5-isopropoxy-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-1-carboxylic acid ethyl ester (175) as a white solid. 1H NMR 400 MHz (DMSO-d6 with trace D2O) δ 8.55 (d, 1H), 8.32 (s, 1H), 8.14 (s, 1H), 7.82 (dd, 1H), 7.74 (t, 1H), 7.34 (t, 1H), 7.28 (s, 1H), 4.73 (m, 2H), 4.39 (s, 2H), 4.12 (m, 2H), 4.06 (q, 2H), 3.46 (m, 1H), 2.92 (m 2H), 1.76 (m, 2H), 1.68 (m, 2H), 1.29 (d, 6H), 1.20 (t, 3H), 1.17 (d, 6H); MS m/z 671 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377921B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-7f2c3fac5fda466c9cfad08f2d382125
출처 메모uspto-grants-2013_02