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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200336Generated: October 30, 2026

2-Bromo-4-fluorobenzene-1-sulfonyl chloride → methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate

https://huagongshe.com/reaction/2200336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-fluorobenzene-1-sulfonyl chlorideHCID 2778216—
Reactantmethyl 7-amino-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylateHCID 89705423—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Productmethyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylateHCID 8970539653.8%

Reaction Steps

2-Bromo-4-fluorobenzenesulfonyl chloride (0.631 g) was added to a solution of methyl 7-amino-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate (Intermediate 6, 0.395 g) in pyridine (20 mL) and DCM (20 mL) and the mixture was allowed to stand at room temperature for 4 days. The resulting solution was evaporated in vacuo, and the residue was partitioned between a mixture of DCM and water and filtered through a phase separator. The filtrate was evaporated to dryness, and the residue was azeotroped with toluene. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 50-100% to give methyl 7-(2-bromo-4-fluorobenzenesulfonylamino)-10H-9-oxa-1,2-diaza-phenanthrene-8-carboxylate (0.408 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359369B2
Source datasetuspto-grants-2016_06
ORD IDord-d0bd37e886934910bb0503b4b67f535e
Source noteuspto-grants-2016_06