Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525004Generated: October 31, 2026

(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid → HCID 86722024, compound

https://huagongshe.com/reaction/525004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acidHCID 2755934—
ReactantHCID 86722025HCID 86722025—
SolventDiisopropyl EtherHCID 7914—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86722024HCID 8672202459.7%

Reaction Conditions

Temperature55 °C

Reaction Steps

1.60 g (6.18 mmol) of 1-amino-N-(3,5-difluorophenyl)-1H-imidazole-2-carboxamide, 1.64 g (8.65 mmol) of (S)-2-(tert-butoxycarbonylamino)butanoic acid and 1.34 g (8.65 mmol) of EDCHCl were dissolved in 45 mL of THF and stirred at 55° C. overnight and at room temperature for 2 days. Then the solvent was evaporated and the crude residue was taken up in ethyl acetate and washed with brine. The organic layer was dried over magnesium sulphate, filtered and the solvent was evaporated. The solid obtained was redissolved in the minimum amount of ethyl acetate and diisopropylether was added until a solid precipitated, which was filtered to furnish 1.51 g (57% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340547B2
Source datasetuspto-grants-2016_05
ORD IDord-37171a4adfef4076abf254a03be6212d
Source noteuspto-grants-2016_05