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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243344Generated: October 31, 2026

Triethylamine → (2-Amino-4,5-difluorophenyl)amide

https://huagongshe.com/reaction/2243344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
ReactantFluoren-4-one-9-carboxylic acid chlorideHCID 87540947—
SolventDichloromethaneHCID 6344—
ProductDiisopropyl EtherHCID 7914—
Product(2-Amino-4,5-difluorophenyl)amideHCID 131727951282%

Reaction Steps

The procedure used in stage 1 of Example 1 is followed, but starting from 1 g of 1,2-diamino-4,5-difluorobenzene, 1.9 ml of triethylamine and 1.7 g of fluoren-4-one-9-carboxylic acid chloride in 50 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 1.4 g of (2-amino-4,5-difluorophenyl)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-6fd5fc1458594209aa813a02f885044f
Source noteuspto-grants-2010_03