Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528183Generated: November 2, 2026

HCID 58736381, compound → HCID 71525424, compound

https://huagongshe.com/reaction/1528183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58736381HCID 58736381—
ReactantC-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamineHCID 89525357—
SolventMethanolHCID 887—
ProductHCID 71525424HCID 7152542470.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 284 mg (0.87 mmol, 1 eq) of 2-hydroxy-3-(2-methoxy-3,4-dioxocyclobut-1-enylamino)-N,N-dimethylbenzenesulfonamide and 318 mg (1.75 mmol) of C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine in 20 ml of methanol was heated at 50° C. for 3 days. The reaction medium was concentrated. The residue was taken up in ethyl acetate and was washed twice with a 1 M aqueous sodium dihydrogen phosphate solution. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. 0.29 g of product was obtained in the form of an ochre solid. Yield=70%, HPLC=98.68%, Mp=123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090596B2
Source datasetuspto-grants-2015_07
ORD IDord-54e8a16d5c28489f8b356f14ac3217ab
Source noteuspto-grants-2015_07