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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294060Generated: October 30, 2026

Methyl [[(methoxycarbonyl)amino](methylthio)methylene]carbamate → Methyl (1-methyl-5-(4-aminophenoxy)-benzimidazol-2-yl)carbamate

https://huagongshe.com/reaction/1294060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl [[(methoxycarbonyl)amino](methylthio)methylene]carbamateHCID 98708—
ReactantN-Methyl-4-(4-nitrophenoxy)-2-nitroanilineHCID 17755333—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl (1-methyl-5-(4-aminophenoxy)-benzimidazol-2-yl)carbamateHCID 1775541712.3%

Reaction Steps

To a mixture of N-methyl-4-(4-nitrophenoxy)-2-nitroaniline (Intermediate 8B -2.10 g, 2.27 mmol) in MeOH (100 mL) was added 5% Pd—C (catalytic amount) and stirred at room temperature under H2 atmosphere. After 7 hrs, the catalyst was removed by filtration then the solvent was evaporated off. The residual mixture was dissolved into MeOH (50 mL) and added 1,3-bis(methoxycarbonyl)-2-methyl-2-thiopseudourea (3.0 g, 14.5 mmol). The mixture was refluxed overnight. The solvent was removed by evaporation and sequence purification on SiO2 column chromatography gave title compound (87.3 mg, 4%): MS m/e 313 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238813B2
Source datasetuspto-grants-2007_07
ORD IDord-a226441c0c6e4a14bc2bb4b2c4e62e57
Source noteuspto-grants-2007_07