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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12330생성일: 2026년 10월 26일

Triethylamine → 4-[(2-Ethoxycarbonyl-ethyl)-indan-5-yl-amino]-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/12330

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
반응물3-(Indan-5-ylamino)-propionic acid ethyl esterHCID 25222875—
용매1-ButanolHCID 263—
생성물4-[(2-Ethoxycarbonyl-ethyl)-indan-5-yl-amino]-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl esterHCID 2522287690%

반응 단계

To a solution of 3-(indan-5-ylamino)-propionic acid ethyl ester (5 g, 21.4 mmol) and ethyl 4-chloro-2-methylthio-5-pyrimidinecarboxylate (5 g, 21.4 mmol) in 40 mL of n-butanol was added triethylamine (3 mL, 21.4 mmol). The solution was stirred at rt for 2 days. The solvent was removed under vacuum. The residue was extracted into EtOAc, washed with water, brine and then dried with Na2SO4. Removal of the solvent and chromatography on silica, eluting with EtOAc/hexanes (1:10-1:6, v/v), gave 8.2 g (90%) of the titled compound as a white solid. 1H NMR (300 MHz, CDCl3) δ (ppm): 8.22 (s, 1H), 7.16 (d, J=7.6 Hz, 1H), 6.95 (s, 1H), 6.87 (d, J=7.6 Hz, 1H), 4.35 (t, 2H), 3.55 (q, 2H), 2.82 (m, 4H), 2.69 (t, 2H), 2.58 (s, 3H), 2.06 (m, 2H), 1.20 (t, 3H), 1.02 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728003B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-388c20312aad4c688e3949a8286aa8af
출처 메모uspto-grants-2010_06