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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284727Generated: November 2, 2026

Acetic Acid → HCID 90052266, compound

https://huagongshe.com/reaction/2284727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
Reactant4-Iodobenzene-1,2-diamineHCID 11207049—
Solvent4-MethylmorpholineHCID 7972—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventIsobutyl chloroformateHCID 62365—
ProductHCID 90052266HCID 9005226678.6%

Reaction Steps

To a solution of N-Boc-glycine (129 mg) in tetrahydrofuran (3.5 mL), isobutyl chloroformate (97 μL) and N-methylmorpholine (81 μL) were added under ice cooling, and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture, 4-iodobenzene-1,2-diamine (200 mg) synthesized according to the method described in WO2010/065668 A1 was added under ice cooling, and the mixture was stirred at room temperature for 1 hour, and then acetic acid (3.5 mL) was added, and the mixture was stirred at 70° C. for 2 hours. 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, 80 to 0% hexane in ethyl acetate) to obtain tert-butyl ((6-iodo-1H-benzo[d]imidazol-2-yl)methyl)carbamate (G4, 216 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-34d64255e62846c5bce3e0374314337e
Source noteuspto-grants-2015_09