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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067233Generated: November 2, 2026

Methanol → (5-Azido-2-methyl-phenyl)-[2-chloro-4-(4-fluoro-phenylamino)-phenyl]-methanone

https://huagongshe.com/reaction/2067233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethanesulfonyl azide, trifluoro-HCID 10986786—
Reactant(5-Amino-2-methyl-phenyl)-[2-chloro-4-(4-fluoro-phenylamino)-phenyl]-methanoneHCID 68418042—
ReactantSodium bicarbonate ethyl acetateHCID 86584982—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(5-Azido-2-methyl-phenyl)-[2-chloro-4-(4-fluoro-phenylamino)-phenyl]-methanoneHCID 86605528—

Reaction Steps

To a suspension of compound 429 (1.00 g, 2.82 mmol) in DCM (5.0 mL) was added a solution of copper(II) sulphate pentahydrate (35.2 mg, 0.14 mmol) in H2O (4.0 mL), and TEA (1.18 mL, 8.45 mmol). The crude trifluoromethansulfonic azide was added slowly under stirring to the reaction mixture followed by by MeOH (5 mL). After 18 h at RT the reaction mixture was poured into a mixture of EtOAc/NaHCO3(aq.). The organic phase was washed with water, brine, filtered and concentrated in vacuo to give the crude product. The crude product was purified by continuous gradient flash chromatography using EtOAc/petroleum ether (40-60) 0:100 to 25:75 as the eluent to afford the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293772B2
Source datasetuspto-grants-2012_10
ORD IDord-221804f92bde4a69a8ef9a763821ec9e
Source noteuspto-grants-2012_10