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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1153861Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1153861

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosgeneHCID 6371—
EduktSulphonyl diisocyanateHCID 77898—
Edukt2-Amino-4,6-dimethoxypyrimidineHCID 118946—
Edukt2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamideHCID 13631887—
Edukt2-(Chloromethyl)benzenesulfonyl isocyanateHCID 20152699—
KatalysatorDiazabicyclo(2.2.2)octaneHCID 136165—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelO-XyleneHCID 7237—
Produkt2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamideHCID 1336461769,6%

Reaktionsschritte

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. 1H nmr δDMSO-d6TMS 12.7 (brd s, 10.50 (s, 1H) 8.13-7.97 (m, 1H), 7.73-7.40 (m, 3H), 5.90 (s, 1H), 5.10 (s, 2H), 3.87 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04486589
Quelldatensatzuspto-grants-1984_12
ORD IDord-d1474643f54545e58f823dac03036fc3
Quellennotizuspto-grants-1984_12