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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23366Generated: October 25, 2026

2-Furancarboxylic acid → HCID 178523861, compound

https://huagongshe.com/reaction/23366

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarboxylic acidHCID 6919—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178511781HCID 178511781—
ProductHCID 178523861HCID 17852386194%

Reaction Conditions

Temperature22 °C

Reaction Steps

2-Furancarboxylic acid (12.6 mg, 0.11 mmol) was activated overnight at about 22° C. with carbonyldiimidazole (0.11 mmol, 0.2M in chloroform). 2-{(1S)-1-Amino-2-[indol-3-yl]ethyl}-4-phenyl-1H-imidazole (0.1 mmol, 0.5M in chloroform) was added to the media and the mixture was stirred for about 12 hours at about 22° C. Aminomethylated resin was then added (50-60 mg, 1.2 mmol/g, Novabiochem) in order to quench the excess of acylating agent for about 12 hours. Purification on silica gel pad (200 mg, Alltech) with ethyl acetate as eluent gave the expected product (37.2 mg, 94%). 1H-NMR (CDCl3, 100 MHz) δ: 8.36 (br s, 1H); 7.67-6.4 (m, 16H); 5.48 (qd, J=7.1 Hz, 1H); 3.6 (ABX system, 2H). LC/MS: m/z=397 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852725B1
Source datasetuspto-grants-2005_02
ORD IDord-53c35be4278545ed89106e250fee70d4
Source noteuspto-grants-2005_02