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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842720Generated: October 25, 2026

Ammonia → HCID 178442312, compound

https://huagongshe.com/reaction/842720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantHexanamideHCID 12332—
ReactantBromineHCID 24408—
Reactant5-amino-1H-imidazole-4-carbonitrileHCID 78777—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178442312HCID 1784423128%

Reaction Steps

1.09 g (11 mmol) of 4-amino-5-cyanoimidazole and 4.39 g (38 mmol) of hexanamide were stirred at 210° C. for 15 hr with heating under an atmosphere of nitrogen. A mixed solvent composed of DMF (200 ml) and water (50 ml) was added thereto. Further, 3.0 ml of benzyl chloride and 3.00 g of potassium carbonate were added thereto. The resultant mixture stirred at 70° C. for 6 hr under heating. After the solvent was removed by vacuum distillation, the residue was taken into water and extracted with dichloromethane. The organic layer was vacuum-concentrated. The residue was purified by silica gel column chromatography (eluent: dichloromethane:methanol=100:1-50:1) to thereby obtain a solid. This solid and 5.00 g of sodium acetate were dissolved in 40 ml of acetic acid. Then, 2 ml of bromine was added to the solution placed in ice bath. Subsequently, the resultant solution was stirred at 70° C. for 6 hours under heating. After the solvent was removed by vacuum distillation, the residue was extracted with ethyl acetate, and the organic layer was vacuum-concentrated. The residue was purified by column chromatography (eluent: dichloromethane:methanol=100:1) to obtain a solid. This solid was added to 20 ml of concentrated hydrochloric acid and heated for 6 hours under refluxing. After the reaction solution was cooled, its pH was adjusted to 8 with aqueous ammonia. The deposited solid was vacuum-filtered, washed with water and then dried to thereby obtain 0.25 g of the captioned compound (yield: 8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376501B1
Source datasetuspto-grants-2002_04
ORD IDord-e3d807c0fc6244a5b7e475e17babfe09
Source noteuspto-grants-2002_04