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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227677Generated: October 30, 2026

Hydrochloric Acid → HCID 18412656, compound

https://huagongshe.com/reaction/2227677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
Reactant1-Methyl-2-aminomethylbenzimidazol-5-yl-carboxylic acid-n-(2-pyridyl)-n-(2-ethoxycarbonylethyl)amide trifluoroacetateHCID 18412483—
SolventWaterHCID 962—
ProductHCID 18412656HCID 18412656—

Reaction Conditions

Temperature100 °C

Reaction Steps

1.5 g (3.25 mmol) of 1-methyl-2-aminomethylbenzimidazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide trifluoroacetate were stirred into 10 ml of N-ethyldiisopropylamine and heated to 100° C. for 15 minutes. After the addition of 720 mg (5.25 mmol) of 2-chloro-5-cyanopyridine, the reaction mixture was heated to 125° C. for 2 hours. After cooling to ambient temperature and stirring with about 20 ml of water, the pH was adjusted to 4 by the addition of 1N hydrochloric acid and the mixture was extracted 3 times with ethyl acetate. The combined organic phases were washed with saline solution and dried over sodium sulfate. After evaporation of the solvent, the crude product was chromatographed on silica gel, eluting first with methylene chloride, later with methylene chloride/ethanol (25:1) and (19:1). The desired fractions were combined and evaporated down.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414008B1
Source datasetuspto-grants-2002_07
ORD IDord-0631a66615a24709aa382f6259864c2c
Source noteuspto-grants-2002_07