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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672258Generated: October 31, 2026

2-Furancarboxylic acid → HCID 67331985, compound

https://huagongshe.com/reaction/1672258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarboxylic acidHCID 6919—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 67333061HCID 67333061—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67331985HCID 6733198587%

Reaction Steps

To a solution of 2-[(4′-Amino-biphenyl-4-carbonyl)-amino]-pentanedioic acid di-tert-butyl ester (350 mg, 0.77 mmol) and 2-Furoic acid (87 mg, 0.77 mmol, 1 equiv.) in DMF (6 mL) was added BOP reagent (409 mg, 0.92 mmol, 1.2 equiv.) and Hunig base (0.16 mL, 0.92 mmol, 1.2 equiv.) under N2. The mixture was stirred at room temperature overnight. Reaction was complete was determined by LC-MS. The reaction mixture was then poured onto cold water. Solid precipitated from the mixture was collected by filtration. The solid was then dissolved in EtOAc, washed with 1N HCl, saturated NaHCO3, and brine, and then dried over MgSO4. After removing the solvent, the solid was dried under vacuum overnight to provide 2-({4′-[(Furan-2-carbonyl)-amino]-biphenyl-4-carbonyl}-amino)-pentanedioic acid di-tert-butyl ester in 87% yield (369 mg). MS (ESI) m/z 549.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998965B2
Source datasetuspto-grants-2011_08
ORD IDord-4726b34873f34329bf4cbecd5b3e289d
Source noteuspto-grants-2011_08