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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368419Generated: October 27, 2026

Benzylamine → 2-Benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridine

https://huagongshe.com/reaction/368419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-(t-Butylamino)-2,3,5,6-tetrafluoropyridineHCID 22121159—
SolventChloroformHCID 6212—
Product2-Benzylamino-4-(t-butyl)amino-3,5,6-trifluoropyridineHCID 2212126784.5%

Reaction Conditions

Temperature115 °C

Reaction Steps

To 10 ml of N-methylpyrrolidone were added 6.8 g of 4-(t-butylamino)-2,3,5,6-tetrafluoropyridine together with 7.2 g of benzylamine, and the mixture was stirred at 115° C. for one day and allowed to cool. After adding 40 ml of chloroform, the mixture was washed three times with 400 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain about 8.0 g of the title compound as a dark green crude oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133284
Source datasetuspto-grants-2000_10
ORD IDord-3b1a55413d774925a66db3234736fdc0
Source noteuspto-grants-2000_10