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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7076Generated: October 28, 2026

Formic Acid → N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-4-[2-(N-formylamino)ethoxy]-3-methoxyphenylacetamide

https://huagongshe.com/reaction/7076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(2-aminoethoxy)-N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-3-methoxyphenylacetamideHCID 22019602—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-4-[2-(N-formylamino)ethoxy]-3-methoxyphenylacetamideHCID 2201959275.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Formic acid (30 mg) is slowly added to acetic anhydride (75 mg), and the mixture is heated with stirring at 60° C. for 2 hours. To the mixture is added dry tetrahydrofuran (0.2 ml), and further added 4-(2-aminoethoxy)-N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-3-methoxyphenylacetamide (100 mg) obtained in Example 62 at −20° C. The mixture is stirred at room temperature for 3 hours. The solvent is evaporated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (80 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084176B2
Source datasetuspto-grants-2006_08
ORD IDord-7a9766c478ba4aec9949a59023cce479
Source noteuspto-grants-2006_08