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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830757Generated: October 26, 2026

2-Isocyanato-1-methoxy-4-methylbenzene → 3-(2-Methoxy-5-methyl-phenyl)-1-methyl-1-pyrazin-2-yl-urea

https://huagongshe.com/reaction/1830757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isocyanato-1-methoxy-4-methylbenzeneHCID 4141520—
ReactantN-Methylpyrazin-2-amineHCID 16767478—
ReactantDichloromethane methanolHCID 21226129—
ReactantEthyl acetate hexaneHCID 21226206—
Solvent1,1-DichloroethaneHCID 6365—
Product3-(2-Methoxy-5-methyl-phenyl)-1-methyl-1-pyrazin-2-yl-ureaHCID 22046431—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 0.3 M stirred solution of 2-methylaminopyrazine (1 equiv.) in dichloroethane at room temperature under nitrogen was added 2-methoxy-5-methylphenylisocyanate (1 equiv.). The reaction was warmed to 80° C. overnight and then cooled to room temperature. In most cases, the product precipitated and was isolated by filtration. Alternatively the product could be isolated by silica gel chromatography using EtOAc/hexane or CH2Cl2/MeOH as eluant. 1H-NMR (400 MHz, CDCl3) δ8.57 (s, 1H), 8.32 (s, 1H), 8.31 (s, 1H), 8.17 (s, 1H), 6.80 (i, 2H), 3.90 (s, 3H), 3.56 (s, 3H), 2.32 (s, 3H). LRMS (ESI, Positive) m/e 273.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067506B2
Source datasetuspto-grants-2006_06
ORD IDord-7757c99411094b4eafe7b8902b065176
Source noteuspto-grants-2006_06