HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nicotinic Acid → N-[4-(3-Fluoronaphthalen-2-yl)-6-imino-1,6-dihydro-1,3,5-triazin-2-yl]pyridine-3-carboximidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nicotinic Acid | HCID 938 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 13373714 | HCID 13373714 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[4-(3-Fluoronaphthalen-2-yl)-6-imino-1,6-dihydro-1,3,5-triazin-2-yl]pyridine-3-carboximidic acid | HCID 11971098 | — |
Reaction Steps
Nicotinic acid (0.58 gram) was dissolved in 10 ml of pyridine, 0.27 gram of methanesulfonyl chloride was added thereto, the mixture was heated to reflux for thirty minutes, 0.5 gram of 2,4-diamino-6-(2-fluoro-3-naphthyl)-s-triazine was added, and the mixture was heated to reflux for four hours. After the reaction was completed, pyridine was evaporated, water was added to the residue, the resulting separated mass was subjected to a column chromatography using 100 grams of silica gel, and eluted with ethyl acetate-benzene (9:1) to afford 2-amino-4-nicotinoylamino-6-(2-fluoro-3-naphthyl)-s-triazine, colourless crystals, melting point 230° to 235° C. (with decomposition). The yield was 0.35 gram.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04554275 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-05c9a79786474d0e97ed86b077b81c93 |
| Source note | uspto-grants-1985_11 |