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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262793Generated: October 26, 2026

Toluene → N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-8-quinolinesulfonamide

https://huagongshe.com/reaction/1262793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant8-QuinolinesulfonamideHCID 94464—
ReactantMethyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13072161—
ReactantTrimethylaluminumHCID 16682925—
SolventDichloromethaneHCID 6344—
ProductN-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-8-quinolinesulfonamideHCID 1307216247.8%

Reaction Steps

To a stirred mixture of 8-quinolinesulfonamide (4.2 g) in 100 ml methylene chloride is added a 2 M toluene solution of trimethylaluminum (15 ml). The resulting solution is stirred under N2 for 45 min. Solid methyl (4-methoxy-6-methylpyrimidin-2-yl)carbamate (4.0 g) is added and the mixture is heated at reflux for 60 hrs. The reaction is quenched sequentially with acetic acid (2 ml) 6 N HCl (5 ml) and water (25 ml). The organic solution is retained, dried with MgSO4, filtered, and is concentrated in vacuo to a crude solid. Washing with methyl acetate afforded 3.6 g of a pale yellow powder m.p. 181°-185° C. The infrared spectrum showed characteristic absorption bands at 3100 and 1700 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04453970
Source datasetuspto-grants-1984_06
ORD IDord-20f12fe65a8a45b2b256904e61c463b9
Source noteuspto-grants-1984_06