Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247790Generated: November 2, 2026

Chloroform → HCID 178454302, compound

https://huagongshe.com/reaction/1247790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTrityl chlorideHCID 6456—
Reactant7-[2,3-bis(tert-butoxycarbonyl)guanidino]-2,3-dihydro-1H-imidazo[1,2-b]pyrazoleHCID 178454303—
SolventPyridineHCID 1049—
ProductHCID 178454302HCID 17845430251.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 7-[2,3-bis(tert-butoxycarbonyl)guanidino]-2,3-dihydro-1H-imidazo[1,2-b]pyrazole (1.83 g) in pyridine (10 ml) was added triphenylmethyl chloride (1.67 g). The mixture was stirred at 50° C. for 5 hours. After cooling, chloroform (50 ml) was added to the reaction mixture, and the mixture was washed successively with 10% aqueous citric acid solution, brine and saturated aqueous sodium hydrogen carbonate solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with 2% methanol/chloroform to give 7-[-2,3-bis(tert-butoxycarbonyl)guanidino]-1-triphenylmethyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole (1.57 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129232B2
Source datasetuspto-grants-2006_10
ORD IDord-57eecb8ac85445bb9be2584f96bb2d08
Source noteuspto-grants-2006_10