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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583867Generated: November 1, 2026

Nicotinic Acid → HCID 70480473, compound

https://huagongshe.com/reaction/1583867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant6-(4-Methoxynaphthalen-1-yl)-1,3,5-triazine-2,4(1H,3H)-diimineHCID 11971099—
ProductHCID 70480473HCID 70480473—

Reaction Steps

Nicotinic acid (2.98 grams) was dissolved in 40 ml of pyridine, 1.39 grams of methanesulfonyl chloride was added thereto, and the mixture was heated to reflux for thirty minutes. Then 2.7 grams of 2,4-diamino-6-(1-methoxy-4-naphthyl)-s-triazine was added thereto, the mixture was heated to reflux for four hours, and the refluxing was continued for three hours more after addition of 0.35 gram of methane sulfonyl chloride. After the reaction was completed, pyridine was evaporated therefrom, water was added to the residue, the crystals separated out were collected by filtration, well washed with water, added to 130 ml of methyl alcohol, the mixture was heated to reflux for twenty minutes, and the crystals were collected by filtration when the solution was still hot. The crystals were then suspended in 50 ml of methyl alcohol, the suspension was heated to reflux for three hours, and dioxane was added to the suspension to afford 2-amino-4-nicotinoyl-amino-6-(1-methoxy-4-naphthyl)-s-triazine, beige needles, melting point 208° to 209° C. The yield was 1.84 grams.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04554275
Source datasetuspto-grants-1985_11
ORD IDord-902bbf6c95de4bb1ba7754631a31dd02
Source noteuspto-grants-1985_11