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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45574Erstellt: 24. Oktober 2026

Ammonia → 2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt)

https://huagongshe.com/de/reaction/45574

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktSodium IodideHCID 5238—
EduktBenzenesulfonic AcidHCID 7371—
Edukt2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonateHCID 58249642—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelIsopropyl AcetateHCID 7915—
Produkt2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt)HCID 7835786349,5%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

10 g of 2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonate (J) obtained in step 3, 5 g of NaI, 20 mL of DMSO and 90 mL of aqueous ammonia were taken in a 500 mL autoclave vessel. The reaction mixture was heated to 80° C. and a pressure of 15 to 17 kg of ammonia maintained for 30-40 hours. The volume of the reaction mass was reduced by vacuum distillation. The RM was washed with 60 mL of IPE. The pH of the RM was adjusted to 10-14 by adding a 50% NaOH solution and extracted three times with 60 mL of MDC. The combined MDC layers were washed with brine, dried over sodium sulphate and distilled under vacuum (crude weight=8 g). The crude mass obtained was dissolved with 10 mL of MDC, and to this 4.5 g benzene sulphonic acid (BSA) dissolved in 30 mL isopropyl acetate (IPAc) was added dropwise over a period of 30 minutes with stirring at RT. The RM was stirred for 30 minutes at RT. The solid obtained was filtered and washed with IPAc and dried under vacuum, resulting in 5 g of the titled compound (Yield=49.5%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541580B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ac1aafe395f44b6fa336ed0ef1904144
Quellennotizuspto-grants-2013_09