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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528191Generated: November 2, 2026

C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine → 3-{[(5-Methylfuran-2-yl)-(3-methyloxetan-3-yl)methyl]amino}-4-(2-oxo-2,3-dihydrobenzooxazol-7-ylamino)cyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/1528191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamineHCID 89525357—
ReactantHCID 89526285HCID 89526285—
SolventMethanolHCID 887—
Product3-{[(5-Methylfuran-2-yl)-(3-methyloxetan-3-yl)methyl]amino}-4-(2-oxo-2,3-dihydrobenzooxazol-7-ylamino)cyclobut-3-ene-1,2-dioneHCID 7152560446%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 0.35 g (1.28 mmol, 1 eq) of 3-ethoxy-4-(2-oxo-2,3-dihydrobenzooxazol-7-ylamino)cyclobut-3-ene-1,2-dione and 0.278 g (1.53 mmol, 1.2 eq) of C-(5-methylfuran-2-yl)-C-(3-methyloxetan-3-yl)methylamine in 6 ml of methanol was heated at 65° C. for 5 hours. The methanol was evaporated off and the residue was chromatographed on silica gel, eluted with 95/5 dichloromethane/methanol. The paste obtained was crystallized from ethyl ether, filtered and dried under vacuum at 40° C. 0.24 g of product was obtained in the form of a beige solid. Yield=46%. HPLC 96.4%, ES+ [410].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090596B2
Source datasetuspto-grants-2015_07
ORD IDord-7649a49b2ff94b158ea93ec87ca8f660
Source noteuspto-grants-2015_07