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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109403Generated: October 30, 2026

Triethylamine → HCID 68861634, compound

https://huagongshe.com/reaction/2109403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,4-Diphenyl-2-furoic acidHCID 150270—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 23062411HCID 23062411—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 68861634HCID 6886163485.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

Triethylamine (5.95 ml) was added dropwise to a mixture of 3,4-diphenyl-2-furancarboxylic acid (compound of Reference Example 33, 3.76 g), 3-(tert-butoxycarbonylamino)-4-methoxybenzoic acid hydrazide (compound of Reference Example 65, 4.00 g), BOP reagent (9.43 g) and DMF (40 ml) at 0° C., and the mixture was stirred overnight at 25° C. After adding water thereto, the reaction solution was diluted with chloroform. The organic layer was then successively washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over MgSO4. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform), thereby giving 6.42 g of the desired compound. Melting point: 137-141° C. (Recrystallized from ethyl acetate/hexane)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514452B2
Source datasetuspto-grants-2009_04
ORD IDord-a1b58b64cabc41a68b0045079928a782
Source noteuspto-grants-2009_04