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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2410024생성일: 2026년 10월 27일

Ethyl isocyanatoacetate → N-{[1-[(3-Cyanophenyl)methyl]-6-hydroxy-2,4-dioxo-3-(phenylmethyl)-1,2,3,4-tetrahydro-5-pyrimidinyl]carbonyl}glycine

https://huagongshe.com/reaction/2410024

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl isocyanatoacetateHCID 76283—
반응물DiisopropylethylamineHCID 81531—
반응물1-benzylpyrimidine-2,4,6(1H,3H,5H)-trioneHCID 268726—
반응물HCID 178472773HCID 178472773—
용매DichloromethaneHCID 6344—
생성물N-{[1-[(3-Cyanophenyl)methyl]-6-hydroxy-2,4-dioxo-3-(phenylmethyl)-1,2,3,4-tetrahydro-5-pyrimidinyl]carbonyl}glycineHCID 6863546273%

반응 단계

Ethyl N-{[6-hydroxy-2,4-dioxo-3-(phenylmethyl)-1,2,3,4-tetrahydro-5-pyrimidinyl]carbonyl}glycinate. Ethyl isocyanatoacetate (2.24 mL, 20 mmoles) was added dropwise to a solution of 1-(phenylmethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione (4.4 g, 20 mmoles) and ethyl diisopropylamine (6.9 mL, 40 mmoles) in dichloromethane (120 mL) and stirred overnight under argon. The mixture was washed with 1 molar hydrochloric acid, water and brine, dried and evaporated. The solid was slurried in diethyl ether, collected, washed with diethyl ether and hexane, dried to give the title compound (5.1 g, 73%). 1H NMR (400 MHz, DMSO-d6) δ ppm 12.13 (br. s., 1 H), 9.84 (br. s., 1 H), 7.13-7.48 (m, 5 H), 4.95 (s, 2 H), 4.17 (d, 2 H), 4.15 (q, 2 H), 1.21 (t, J=7.20 Hz, 3 H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08815884B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-1314b3d30f8f4e9188c542534b71b0bb
출처 메모uspto-grants-2014_08