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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243340Generated: October 31, 2026

Triethylamine → (2-Amino-5-chloro-4-fluorophenyl)amide

https://huagongshe.com/reaction/2243340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-5-fluoro-1,2-phenylenediamineHCID 735773—
ReactantFluoren-4-one-9-carboxylic acid chlorideHCID 87540947—
SolventDichloromethaneHCID 6344—
ProductDiisopropyl EtherHCID 7914—
Product(2-Amino-5-chloro-4-fluorophenyl)amideHCID 131727949301.9%

Reaction Steps

The procedure used in stage 1 of Example 1 is followed, but starting from 1 g of 1,2-diamino-4-chloro-5-fluorobenzene, 1.75 ml of triethylamine and 1.5 g of fluoren-4-one-9-carboxylic acid chloride in 45 ml of dichloromethane. After stirring for 20 hours at room temperature, the precipitate that formed is filtered off, and washed with dichloromethane, with water, then with a 10% saturated aqueous solution of sodium hydrogen carbonate and, finally, with water. After formation of a paste with diisopropyl ether, in this way we obtain 1.5 g of (2-amino-5-chloro-4-fluorophenyl)amide of 9-oxo-9H-fluorene-4-carboxylic acid, in the form of a yellow powder, which is used as it is in the following stage, with the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674795B2
Source datasetuspto-grants-2010_03
ORD IDord-bd376865731c4017a6a231c262439b35
Source noteuspto-grants-2010_03