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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469827Generated: October 29, 2026

Water → 4-{7-[4-(1,1-Dioxo-thiomorpholin-4-ylmethyl)-3,5-difluoro-phenyl]-benzooxazol-2-ylamino}-2,N,N-trimethyl-benzamide

https://huagongshe.com/reaction/469827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-[2,6-Difluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-thiomorpholine 1,1-dioxidHCID 59392800—
Reactant4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamideHCID 67457821—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-{7-[4-(1,1-Dioxo-thiomorpholin-4-ylmethyl)-3,5-difluoro-phenyl]-benzooxazol-2-ylamino}-2,N,N-trimethyl-benzamideHCID 59144330—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 0.1 g (0.267 mmol) 4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamide, 0.114 g (0.294 mmol) 4-[2,6-difluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-thiomorpholine 1,1-dioxid and 174 mg K3PO4 are dissolved in 5 ml 1,2-dimethoxy-ethane, water (0.1 ml) is added and a stream of argon is bubbled through the mixture in order to exclude oxygen from the reaction mixture. Tetrakis (triphenylphosphine) palladium (0.0095 g, 0.0082 mmol) is added and the reaction mixture is stirred at 100° C. for 8 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), followed by recrystallisation diethylether/methanol to afford the title compound as white crystals. Rt=2.13 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: 555 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629168B2
Source datasetuspto-grants-2014_01
ORD IDord-e1317406ee524d3f8d3c856d24ed7f80
Source noteuspto-grants-2014_01