Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103755Generated: October 26, 2026

N-Ethyl cyclohexylamine → N-cyclohexyl-2-[2-(2,2-dimethylpropanoyl)-5-methoxy-1-benzofuran-3-yl]-N-ethylacetamide

https://huagongshe.com/reaction/2103755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Ethyl cyclohexylamineHCID 21609—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant[2-(2,2-Dimethylpropanoyl)-5-methoxy-1-benzofuran-3-yl]acetic acidHCID 57804476—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
ProductN-cyclohexyl-2-[2-(2,2-dimethylpropanoyl)-5-methoxy-1-benzofuran-3-yl]-N-ethylacetamideHCID 11395458—

Reaction Conditions

Temperature40 °C

Reaction Steps

Dissolve a mixture of 17 mg [2-(2,2-dimethylpropanoyl)-5-methoxy-1-benzofuran-3-yl]acetic acid from the Step B Example 1 and 18.5 mg HOBt in 1 mL dry DMF. Add 13.2 μL N-ethylcyclohexylamine followed by 23.0 mg EDC and 35 μL DIEA. This solution was heated at 40° C. for 2 hours. It was purified directly on RP-HPLC using 65-100% MeCN gradient. The fractions containing pure product were pooled and lyophilized to give the title compound. LC-MS: 4.34 min. (m/Z=400.2, 422.1, 316.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576122B2
Source datasetuspto-grants-2009_08
ORD IDord-5ee7cc99e42b409f9ca0471f9189dbfd
Source noteuspto-grants-2009_08