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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284668Generated: November 4, 2026

Acetic Acid → HCID 90052209, compound

https://huagongshe.com/reaction/2284668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
Reactant4-Nitro-1,2-phenylenediamineHCID 5111791—
Solvent4-MethylmorpholineHCID 7972—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventIsobutyl chloroformateHCID 62365—
ProductHCID 90052209HCID 9005220982.1%

Reaction Steps

To a solution of N-Boc-glycine (571 mg) in tetrahydrofuran (16 mL), isobutyl chloroformate (428 μL) and N-methylmorpholine (358 μL) were added under ice cooling, and the mixture was stirred at the same temperature for 20 minutes. To the reaction mixture, 4-nitro-1,2-phenylenediamine (500 mg) was added under ice cooling, and the mixture was stirred at room temperature for 3 hours and 30 minutes. To the reaction mixture, acetic acid (16 mL) was added, and the mixture was stirred at 70° C. for 3 hours and 30 minutes. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed successively with saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 100 to 0% hexane in ethyl acetate) to obtain tert-butyl ((6-nitro-1H-benzo[d]imidazol-2-yl)methyl)carbamate (C19, 782 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-28c4baa53ff04c01a836f5406c058878
Source noteuspto-grants-2015_09