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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420473Generated: November 1, 2026

Cyclohexylamine → 3-Benzyloxy-6-methyl-4-oxo-4H-pyran-2-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/420473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-(benzyloxy)-6-methyl-4-oxo-4H-pyran-2-carboxylic acidHCID 9856497—
SolventDimethylformamideHCID 6228—
Product3-Benzyloxy-6-methyl-4-oxo-4H-pyran-2-carboxylic acid cyclohexylamideHCID 8661179761%

Reaction Steps

1,1′-carbonyldiimidazole (1.99 g, 12.30 mmol) was added to a solution of the 3-(benzyloxy)-6-methyl-4-oxo-4H-pyran-2-carboxylic acid (2.0 g, 7.69 mmol) in dimethylformamide (DMF, 18 ml) at room temperature. The resulting solution was heated at 40°-50° C. for 3 hrs. A light yellow solution was observed. Cyclohexylamine (1.23 ml, 10.76 mmol) was then added. The resulting mixture was stirred at room temperature for overnight. The DMF was removed under reduced pressure to give light yellow oil as a crude product, which was purified by flash column chromatography (elution gradient: from 1:1 ethyl acetate/hexane to 10% methanol in ethyl acetate) to yield the titled compound (1.60 g, yield 61%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097624B2
Source datasetuspto-grants-2012_01
ORD IDord-1b89491ab49f4956a726c90df2609b3f
Source noteuspto-grants-2012_01