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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622101Generated: October 30, 2026

(Diethylamino)sulfur trifluoride → 8-chloro-5-(4-chlorophenyl)-5-fluoro-5H-indeno[1,2-d]pyrimidine

https://huagongshe.com/reaction/622101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantPotassium BicarbonateHCID 516893—
Reactant8-chloro-5-(4-chlorophenyl)-5H-indeno[1,2-d]pyrimidin-5-olHCID 14257087—
SolventDichloromethaneHCID 6344—
Product8-chloro-5-(4-chlorophenyl)-5-fluoro-5H-indeno[1,2-d]pyrimidineHCID 1425709775.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3.0 g of 8-chloro-5-(4-chlorophenyl)-5H-indeno[1,2-d]pyrimidin-5-ol in 50 ml of methylene chloride was cooled to 0° C. under a nitrogen atmosphere. Approximately 2.7 g of diethylaminosulfur trifluoride were added and the reaction was stirred overnight. The mixture was poured into an iced solution of potassium bicarbonate and extracted with ethyl acetate. The organic extract was washed with a sodium bicarbonate solution and a sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. Crystallization from ethyl acetate/isooctane provided 2.29 g of the desired title product, m.p. 236°-237° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04769378
Source datasetuspto-grants-1988_09
ORD IDord-ea165d1e36bf40e283f87d7dc47a953e
Source noteuspto-grants-1988_09