Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218216Generated: October 30, 2026

Oxazole → HCID 57378193, compound

https://huagongshe.com/reaction/218216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxazoleHCID 9255—
ReactantHCID 59428119HCID 59428119—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 57378193HCID 57378193—

Reaction Steps

To a cooled (−78° C.) solution of n-BuLi (0.5 mL, 2.5 M solution in hexanes) in THF (3 mL) was added oxazole (0.1 mL, 1.5 mmol) via dropwise addition and the solution was stirred for 30 minutes. ZnCl2 solution (3.9 mL, 0.5 M in THF) was then added and the reaction mixture was warmed to room temperature and stirred an additional 2 hours. Pd(PPh3)4 (20 mg, 0.015 mmol) and 4-tert-butyl-N-[4-chloro-2-(4-iodo-5-methyl-[1,2,3]triazol-1-yl)-phenyl]-benzenesulfonamide (synthesized according to general procedure P, 77 mg, 0.15 mmol) were then added and the reaction mixture was heated at 80° C. overnight. The reaction mixture was subsequently diluted with EtOAc (25 mL) and the combined organics were washed with water (20 mL), dried (Na2SO4), and concentrated in vacuo. The crude product was purified by preparative TLC to afford the title compound: MS (ES) M+H expected 472.1, found 472.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198309B2
Source datasetuspto-grants-2012_06
ORD IDord-62df78ecb9994c8eb1fc0fa82443c703
Source noteuspto-grants-2012_06