HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714474Generated: October 29, 2026
Hydrochloric Acid → HCID 56592010, compound
https://huagongshe.com/reaction/714474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Benzoic acid, 3-(hydroxymethyl)- | HCID 185629 | — |
| Reactant | 2-Amino-4-phenyl-6-phenylsulfanylpyridine-3,5-dicarbonitrile | HCID 4165107 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 56592010 | HCID 56592010 | — |
Reaction Steps
4.72 g (42.06 mmol) of potassium tert-butoxide were suspended in 25 ml of 1,2-dimethoxyethane. After addition of 1.73 g (10.51 mmol) of 3-(hydroxymethyl)benzenecarboxylic acid (Example 66A) and 1.72 g (5.26 mmol) of 2-amino-4-phenyl-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile (Example 36A), the mixture was stirred at 60° C. overnight. After cooling of the reaction mixture, 50 ml of water were added. With ice-cooling, the clear solution was acidified to pH 6-7 using conc. hydrochloric acid. The solution was evaporated. Purification was by column chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 1/1, finally acetonitrile/water 10/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187428B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-46a0d27483334464b0612eabc200768e |
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| Source note | uspto-grants-2015_11 |
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