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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788796Generated: October 25, 2026

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

https://huagongshe.com/reaction/1788796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
ReactantN-(3-chloropyridazine-6-sulfonyl)phenylcarbamateHCID 86741701—
Solvent1,4-DioxaneHCID 31275—
ProductN-(3-Chloropyridazine-6-sulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureaHCID 2127574343.3%

Reaction Steps

A mixture of 14.2 g of N-(3-chloropyridazine-6-sulfonyl)phenylcarbamate and 6.3 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine are refluxed for 1 hour in 120 ml of absolute dioxan. When the reaction is complete, the mixture is concentrated in vacuo and the residue is taken up in a saturated aqueous solution of sodium bicarbonate and the insoluble constituents are extracted with methylene chloride. The aqueous phase is acidified with dilute hydrochloric acid and extracted with methylene chloride. The methylene chloride solution is dried over sodium sulfate and concentrated, affording 7 g of the compound of the above formula with a melting point of 135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684730
Source datasetuspto-grants-1987_08
ORD IDord-ae4597ad267b47eb9940dcaad6564230
Source noteuspto-grants-1987_08