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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 363987Erstellt: 25. Oktober 2026

Pyridine → Pyridazinyl carbamate

https://huagongshe.com/reaction/363987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktPyridazineHCID 9259—
EduktPhenyl chloroformateHCID 15891—
EduktAminopyridazineHCID 230373—
LösungsmittelTriethylamineHCID 8471—
ProduktPyridazinyl carbamateHCID 20239911—

Reaktionsschritte

The reaction of a haloformate, such as phenyl chloroformate, and a pyridazineamine generally is carried out by combining a slight excess of haloformate with the pyridazine in an organic solvent, such as pyridine or triethylamine, and stirring the mixture for about 1 to about 24 hours at a temperature of about 0° to about 30° C. The product of the reaction, a pyridazinyl carbamate, is generally isolated by acidifying the reaction mixture, for instance by the addition of a mineral acid, such as hydrochloric acid or sulfuric acid, and collecting by filtration the precipitate which forms. The carbamate normally needs no further purification, but if desired it can be crystallized from common solvents, such as benzene, acetone, ethyl acetate, and the like.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04604127
Quelldatensatzuspto-grants-1986_08
ORD IDord-492eae2209534bc4af5cb4e1d76c9009
Quellennotizuspto-grants-1986_08