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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187342Generated: October 29, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 11016088, compound

https://huagongshe.com/reaction/2187342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCarbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl esterHCID 10945667—
ReactantHCID 11108888HCID 11108888—
SolventAcetonitrileHCID 6342—
ProductHCID 11016088HCID 11016088—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 1.50 g of 5-(2-dimethylamino-1-azaethenyl)-2-methoxycarbonylbenzenesulfonamide, 1.61 g of 4,6-dimethoxy-2-phenoxycarbonylaminopyrimidine, 32 ml of acetonitrile and 0.83 ml of DBU is stirred initially at 0° C. and then at room temperature until the reaction has ended. The reaction mixture is then concentrated under reduced pressure. The residue is taken up in water and washed with diethyl ether. The aqueous phase is carefully acidified with conc. hydrochloric acid (pH 6) and the sulfonylurea precipitate is separated off, washed with diisopropyl ether and water and dried. This affords 1.89 g of the desired sulfonylurea, melting point 73-75° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410482B1
Source datasetuspto-grants-2002_06
ORD IDord-6a4ad6ed00144a1396842a210de12e0f
Source noteuspto-grants-2002_06