Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583127Generated: October 29, 2026

Triethylamine → HCID 15817390, compound

https://huagongshe.com/reaction/583127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
ReactantHCID 15817388HCID 15817388—
SolventAcetonitrileHCID 6342—
ProductHCID 15817390HCID 15817390—

Reaction Steps

1.58 ml (11.38 mmol) of triethylamine and 0.88 g (5.68 mmol) of 4-(trifluoromethyl)benzyl bromide, in solution in 5 ml of acetonitrile, are successively added at room temperature, with magnetic stirring and under an argon atmosphere, to a solution of 1 g (2.84 mmol) of 5-(8-amino-7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)-3-(piperidin-4-yl)-1,3,4-oxadiazol-2(3H)-one in 60 ml of acetonitrile and the mixture is stirred for 2 h. The solvent is evaporated under reduced pressure, the residue is taken up in chloroform, the solution is washed a number of times with water and dried and the solvent is evaporated under reduced pressure. The residue is crystallized from acetone and 1.14 g of white solid are obtained. Melting point: 198° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929089
Source datasetuspto-grants-1999_07
ORD IDord-989a6851f9b548b1a2204b9b143ff1d7
Source noteuspto-grants-1999_07