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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877945Generated: October 30, 2026

Ethyl isocyanate → HCID 58827101, compound

https://huagongshe.com/reaction/1877945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
Reactant3-amino-4-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)benzonitrileHCID 58827043—
SolventDimethylformamideHCID 6228—
ProductHCID 58827101HCID 58827101—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 3-Amino-4-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)benzonitrile (0.090 g, 0.420 mmol), given as example 6B, and DMF (5 mL) is added ethylisocyanate (0.040 mL, 0.510 mmol). The solution is heated to 70° C. in a microwave reactor for 1.5 h followed by heating at 70° C. in an oil bath overnight. The solution is then concentrated and the residue purified via flash chromatography (1-10% MeOH/CH2Cl2) to give 1-[5-Cyano-2-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)phenyl]-3-ethylurea. MS (ESI) m/z 296.1 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.16 (t, J=7.2 Hz, 3 H), 2.47-2.62 (m, 1 H), 2.82-3.04 (m, 2 H), 3.05-3.17 (m, 1 H), 3.21-3.33 (m, 2 H), 5.63 (app t, J=6.8 Hz, 1 H), 5.80 (br s, 1 H), 6.82 (s, 1 H), 6.91 (d, J=8.1 Hz, 1 H), 7.30 (dd, J=8.1, 1.5 Hz, 1 H), 7.39 (s, 1 H), 7.53 (br s, 1 H), 7.97 (d, J=1.3 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-58319ec52d4f4b0db3b08f06e53916a3
Source noteuspto-grants-2012_11