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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469820Generated: October 29, 2026

4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamide → 4-[7-(3-Fluoro-4-morpholin-4-ylmethyl-phenyl)-benzooxazol-2-ylamino]-2,N,N-trimethyl-benzamide

https://huagongshe.com/reaction/469820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamideHCID 67457821—
Reactant4-(2-Fluoro-4-trimethylstannanyl-benzyl)-morpholineHCID 67458083—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-[7-(3-Fluoro-4-morpholin-4-ylmethyl-phenyl)-benzooxazol-2-ylamino]-2,N,N-trimethyl-benzamideHCID 59144312—

Reaction Conditions

Temperature150 °C

Reaction Steps

0.1 g (0.267 mmol) 4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamide and 0.17 g (0.305 mmol) 4-(2-fluoro-4-trimethylstannanyl-benzyl)-morpholine are dissolved in 2 ml 1,2-dimethoxy-ethane and a stream of argon is bubbled through the mixture in order to exclude oxygen from the reaction mixture. Tetrakis (triphenylphosphine) palladium (0.020 g, 0.016 mmol) is added and the reaction mixture is stirred at 150° C. for 1 h. After that the reaction mixture is poured on water and extracted 3× with EtOAc. The combined organic layers are washed with water and saturated NaCl solution, dried over MgSO4, filtered and the filtrate is concentrated in vacuo. The residue is purified by chromatography (silicagel, EtOAc:MeOH=95:5; column chromatography followed by thick-layer chromatography) to afford the title compound. Rt=1.67 min (Waters Symmetry C8, 2.1×50 mm, detection 210-250 nM, 5% to 100% CH3CN in H2O in 2 min+0.05% TFA, flow rate 1.0 ml/min); MS: 375 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629168B2
Source datasetuspto-grants-2014_01
ORD IDord-894fdc4cb1594457a4992f6135d91a5b
Source noteuspto-grants-2014_01