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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279751Generated: October 27, 2026

Phosgene → 2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/279751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantSulphonyl diisocyanateHCID 77898—
Reactant2-Amino-4,6-dimethoxypyrimidineHCID 118946—
Reactant2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamideHCID 13631887—
Reactant2-(Chloromethyl)benzenesulfonyl isocyanateHCID 20152699—
CatalystDiazabicyclo(2.2.2)octaneHCID 136165—
SolventAcetonitrileHCID 6342—
SolventO-XyleneHCID 7237—
Product2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamideHCID 1336461769.6%

Reaction Steps

A solution of 2-(chloromethyl)-N-(butylaminocarbonyl)benzene sulfonamide (1.33 g, 4.38 mmol) and diazabicyclo[2.2.2]octane (5 mg) in xylene (12 ml) was heated at reflux and contacted in portions with phosgene (1.0 ml. condensed phase). After 2.0 hrs at reflux, the mixture was cooled to room temperature, decanted, and volatiles were removed to give 1.56 g of crude product. The IR spectrum of 2-(chloromethyl)benzenesulfonyl isocyanate featured a strong band at 2250 cm-1. The crude sulfonyl isocyanate was contacted with acetonitrile (10 ml) and 2-amino-4,6-dimethoxypyrimidine (0.68 g, 4.4 mmol) and stirred for 16 hrs. Filtration gave 1.18 g of white solid, mp 192°-193°. The sample was dissolved in 0.5N NaOH, filtered and pH adjusted to 6.5. The mixture was cooled and filtered and the solid washed with ice water and dried to give 0.90 g of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04586952
Source datasetuspto-grants-1986_05
ORD IDord-93e642c1e24744088cda946e15a2bb3a
Source noteuspto-grants-1986_05