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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25553Erstellt: 23. Oktober 2026

Pyridine → HCID 178485978, Verbindung

https://huagongshe.com/de/reaction/25553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktQuinolineHCID 7047—
EduktDiphosgeneHCID 10426—
Edukt2,4-DifluorophenolHCID 123051—
Edukt[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-amineHCID 22567629—
EduktSodium bicarbonate ethyl acetateHCID 86584982—
EduktHCID 178484847HCID 178484847—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178485978HCID 178485978—

Reaktionsschritte

A solution of 1.5 mmol trichloromethyl-chloroformate (diphosgene) in 20 ml CH2Cl2 was treated at 0° C. with 3 mmol of 2,4-difluoro-phenol and 3 mmol quinoline and then stirred for 3 h at room temperature. The reaction was then cooled (0° C.) and a solution of 1 mmol [4-(4-Bromo-butoxy)-cyclohexyl]-methyl-amine (privously prepared from trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-amine hydrochloride by extraction with aqueous NaHCO3/EtOAc) and 2.5 mmol pyridine in 3 ml CH2Cl2 was added. The reaction was stirred over night at room temperature, evaporated to give crude trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 2,4-difluoro-phenyl ester which was used directly in the next step, see Example 12.39-12.44.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858651B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-d3a966ad51af4afeb9e5f375319b6d86
Quellennotizuspto-grants-2005_02