HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714475Generated: November 1, 2026
Water → 4-({[6-amino-3,5-dicyano-4-(4-fluorophenyl)pyridin-2-yl]oxy}methyl)-N-methylpyridine-2-carboxamide
https://huagongshe.com/reaction/714475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-4-[4-fluorophenyl]-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile | HCID 11739479 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-(hydroxymethyl)-N-methylpyridine-2-carboxamide hydrochloride hydrate | HCID 66631382 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-({[6-amino-3,5-dicyano-4-(4-fluorophenyl)pyridin-2-yl]oxy}methyl)-N-methylpyridine-2-carboxamide | HCID 66631060 | — |
Reaction Steps
1.62 g (14.44 mmol) of potassium tert-butoxide were suspended in 10 ml of 1,2-dimethoxyethane. After addition of 1.44 g (8.66 mmol) of 4-(hydroxymethyl)-N-methylpyridine-2-carboxamide hydrochloride monohydrate (Example 40A) and 1.00 g (2.89 mmol) of 2-amino-4-[4-fluorophenyl]-6-(phenylsulfanyl)pyridine-3,5-dicarbonitrile (Example 38A), the mixture was stirred at 60° C. for 2 h and at RT overnight. 30 ml of water were added to the reaction mixture. The precipitate was filtered off and washed with water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09187428B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-65e7bb050b2d4d8da5ff9215051d3197 |
|---|
| Source note | uspto-grants-2015_11 |
|---|