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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528209Generated: November 3, 2026

C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine → HCID 71525973, compound

https://huagongshe.com/reaction/1528209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamineHCID 89525357—
ReactantHCID 89534509HCID 89534509—
SolventMethanolHCID 887—
ProductHCID 71525973HCID 7152597393%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 500 mg (1.27 mmol) of methyl (S)-1-[2,6-difluoro-3-(2-methoxy-3,4-dioxocyclobut-1-enylamino)benzoyl]-pyrrolidine-2-carboxylate and 344 mg (1.90 mmol, 1.5 eq) of C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine in 25 ml of methanol was heated at 60° C. and was then stirred at ambient temperature overnight. The reaction medium was concentrated. The residue was taken up with 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. 0.64 g of methyl (S)-1-[2,6-difluoro-3-(2-{[(5-methylfuran-2-yl)-(3-methyloxetan-3-yl)methyl]amino}-3,4-dioxocyclobut-1-enylamino)benzoyl]pyrrolidine-2-carboxylate was obtained. Yield=93%, Mp=122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090596B2
Source datasetuspto-grants-2015_07
ORD IDord-d5db4ab54bf4460fbeb8cb9c8eef650b
Source noteuspto-grants-2015_07