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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537869Generated: October 29, 2026

N-(3-Aminophenyl)methanesulfamide → HCID 71060627, compound

https://huagongshe.com/reaction/537869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminophenyl)methanesulfamideHCID 2734262—
ReactantHCID 71060236HCID 71060236—
SolventIsopropanolHCID 3776—
ProductHCID 71060627HCID 7106062784.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(2-chlorooxazol-5-yl)-2-fluorobenzonitrile 39 (0.225 g, 1.01 mmol) and commercially available N-(3-aminophenyl)methanesulfonamide 6 (0.188 g, 1.01 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Reaction mixture was evaporated and crude product was purified using MPLC (Biotage) silica column (Biotage) (Acetone/hexane as an eluent) to provide N-(3-((5-(4-cyano-3-fluorophenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide 40 (0.319 g, 84% yield) as a solid. MS (ES) m/z 373 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865709B2
Source datasetuspto-grants-2014_10
ORD IDord-124e0aa7673942059381e54ca13ff6c7
Source noteuspto-grants-2014_10