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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914902Generated: October 29, 2026

Potassium → Dimethylsulfamic acid [4,5-difluoro-6-(2-fluoro-4-bromo-phenylamino)-benzooxazol-7-yl]-amide

https://huagongshe.com/reaction/1914902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassiumHCID 5462222—
ReactantCyclopropanesulfonic acid [4,5-difluoro-6-(2-fluoro-4-iodo-phenylamino)-benzooxazol-7-yl]-amideHCID 53241452—
Reactant6-(4-Bromo-2-fluoro-phenyl)-4,5-difluoro-7-oxo-6,7-dihydro-imidazo[4',5':3,4]benzo[1,2-d]oxazole-8-sulfonic acid dimethylamideHCID 68313528—
ProductDimethylsulfamic acid [4,5-difluoro-6-(2-fluoro-4-bromo-phenylamino)-benzooxazol-7-yl]-amideHCID 53241454—

Reaction Steps

Compound 1F was prepared from 6-(4-bromo-2-fluoro-phenyl)-4,5-difluoro-7-oxo-6,7-dihydro-imidazo[4′,5′:3,4]benzo[1,2-d]oxazole-8-sulfonic acid dimethylamide (I-24a: 100 mg, 0.203 mmol) and potassium trimethylsilonolate (39 mg, 0.305 mmol) using procedures analogous to those described above for Compound 1A to afford 30 mg of the product (29% yield). H1NMR (CDCl3, 300 MHz): δ 8.14 (s, 1H), 7.11-7.24 (m, 2H), 7.12 (dt, 1H), 6.79 (s, 1H), 6.58-6.48 (m, 1H), 2.90 (s, 6H). LCMS: 95.77%, m/z=462.9 (M−2). HPLC: 96.26%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614239B2
Source datasetuspto-grants-2013_12
ORD IDord-99d712d2b7524772bbcea9e2daae0204
Source noteuspto-grants-2013_12