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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913615Generated: October 30, 2026

Tetrahydrofuran → 2-(3-Iodopyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/1913615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantN-[2-hydroxy-5-(trifluoromethyl)phenyl]-3-iodoisonicotinamideHCID 66880065—
SolventTolueneHCID 1140—
Product2-(3-Iodopyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688059780.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 1.81 g of N-[2-hydroxy-5-(trifluoromethyl)phenyl]-3-iodoisonicotinamide, 20 ml of tetrahydrofuran and 1.34 g of triphenylphosphine, 2.22 g of 40% toluene solution of diethyl azodicarboxylate was added dropwise at room temperature. The reaction mixture was stirred while heating at 50° C. for one hour. The reaction mixture was cooled to room temperature, and then the reaction mixture was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 1.40 g of 2-(3-iodopyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 29”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-a10d8006e1f245419c347e8ff91da38f
Source noteuspto-grants-2013_12