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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247469Generated: October 26, 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/247469

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 numberUS04707551
Source datasetuspto-grants-1987_11
ORD IDord-cc3cf87295054356b17909d3b9a248d0
Source noteuspto-grants-1987_11