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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410045Generated: October 31, 2026

Ethyl isocyanatoacetate → HCID 24830240, compound

https://huagongshe.com/reaction/2410045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanatoacetateHCID 76283—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18375361HCID 18375361—
SolventDichloromethaneHCID 6344—
ProductHCID 24830240HCID 24830240—

Reaction Steps

-{[6-Hydroxy-1,3-bis(3-methylbutyl)-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl]carbonyl}glycine. A mixture of 1,3-bis(3-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione (1.2 g, 4.47 mmoles) and diisopropylethylamine (1.56 mL, 8.94 mmoles) was stirred in dichloromethane (30 mL) and treated with ethyl isocyanatoacetate (501 uL, 4.47 mmoles). The mixture was stirred for 5 hours, washed with 1 molar hydrochloric acid (×2), evaporated, taken up in ethanol-6 molar sodium hydroxide and stirred overnight. The mixture was acidified and extracted into ethyl acetate (×2). The extracts were washed with 1 molar hydrochloric acid evaporated, dried and evaporated. The title compound was recrystallized from acetic acid (430 mg, 26%). 1H NMR (400 MHz, DMSO-d6) δ ppm 13.09 (br. s, 1 H), 10.11 (s, 1 H), 4.09-4.16 (m, 2 H), 3.77-3.86 (m, 4 H), 1.51-1.62 (dt, J=13.29, 6.59, 6.59, 6.59, 6.59 Hz, 2 H), 1.42 (q, J=7.07 Hz, 4 H), 0.91 (d, J=6.57 Hz, 12 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815884B2
Source datasetuspto-grants-2014_08
ORD IDord-6e7e951143ab4f6aae06267469ccbb34
Source noteuspto-grants-2014_08