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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381386Generated: October 30, 2026

Ammonium formate → HCID 15896318, compound

https://huagongshe.com/reaction/381386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1h-Benzimidazole-1-carboxylic acid,4-methyl-5-nitro-,1,1-dimethylethyl esterHCID 15896317—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 15896318HCID 15896318—

Reaction Conditions

Temperature50 °C

Reaction Steps

5-Amino-1-tert-butoxycarbonyl-4-methylbenzimidzole. To a solution of 8 g of 1-tert-butoxycarbonyl-4-methyl-5-nitrobenzimidazole in 40 mL of methanol and 400 mL of ethylacetate are added 500 mg of 10% palladium-on-carbon and 7.27 g of ammonium formate. The mixture is stirred at 50° C. for 2 hours, then filtered on Celite, with a methanol wash of the solids. The filtrate is rotary evaporated and the residue partitioned between water and ethyl acetate. The organic layer is washed with saturated ammonium chloride, dried over magnesium sulfate, filtered and rotary evaporated to afford 5-amino-1-tert-butoxycarbonyl-4-methylbenzimidazole as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306877B1
Source datasetuspto-grants-2001_10
ORD IDord-b4a3fe1cd93245efa635c23f2025facb
Source noteuspto-grants-2001_10