HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992647Generated: October 31, 2026
Hydrochloric Acid → HCID 18412656, compound
https://huagongshe.com/reaction/992647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Reactant | HCID 131721872 | HCID 131721872 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18412656 | HCID 18412656 | — |
Reaction Steps
1.5 g (3.25 mmol) of 1-methyl-2-aminomethyl-benzimidazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)-amide-trifluoracetate were stirred into 10 ml of N-ethyl-diisopropylamine and heated to 100° C. for 15 minutes. After the addition of 720 mg (5.25 mmol) of 2-chloro-5-cyano-pyridine 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 sulphate. 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469039B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-6bf4e0c1777240ff9c0ae111bdbab7d9 |
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| Source note | uspto-grants-2002_10 |
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