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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292695Generated: October 30, 2026

Hydrochloric Acid → HCID 67572402, compound

https://huagongshe.com/reaction/1292695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-[(5-Formylimidazol-1-yl)methyl]benzonitrileHCID 10632289—
ReactantHCID 18660148HCID 18660148—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 67572402HCID 67572402—

Reaction Steps

Through a solution of the product from Step I (533 mg, 1.47 mmol) in 20 mL of EtOAc at 0° C. was bubbled HCl gas. The saturated solution was warmed to room temperature and stirred for 40 minutes, then concentrated in vacuo. To a solution of this amine salt in 6 mL of 1:1 MeOH/THF at 0° C. was added the aldehyde from Step E (325 mg, 1.54 mmol) and 0.05 mL of acetic acid. After one hour, sodium cyanoborohydride was added (97 mg, 1.54 mmol), and the solution was allowed to warm to room temperature overnight. After ~16 hours, the reaction was poured into EtOAc, washed with sat. aq. NaHCO3 and brine, dried (Na2 SO4), filtered, and concentrated in vacuo. The resulting product was purified by silica gel chromatography (1-2% MeOH/CHCl3). A portion of this was taken up in EtOAc/Et2O and treated with excess HCl gas, then stripped to provide the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756528
Source datasetuspto-grants-1998_05
ORD IDord-12a37a28a77c469789949c7f2aa23c62
Source noteuspto-grants-1998_05