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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725186Generated: October 26, 2026

Triethylamine → HCID 178438858, compound

https://huagongshe.com/reaction/1725186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCarbonic acid-guanidine (1:1)HCID 286947—
Reactant[2-Phenyl-5-(4-propyl-cyclohexyl)-pyrrol-1-yl]-acetic acidHCID 57423722—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178438858HCID 178438858145.2%

Reaction Steps

To a solution of 0.91 g (2.8 mmol) [2-phenyl-5-(4-propyl-cyclohexyl)-pyrrol-1-yl]-acetic acid in 28 mL anhydrous DMF was added 2.27 g (14 mmol) carbonyldiimidazole. The reaction was stirred at room temperature for 50 min, upon which time was added 2.52 g (14 mmol) guanidine carbonate, 0.17 g (1.4 mmol) 4-dimethylaminopyridine, and 2.83 g (28 mmol) triethylamine. The reaction was stirred at room temperature over 16 hr. The solution was filtered to remove the precipitate that formed, was diluted with ethyl acetate, and was washed three times with brine. Drying over MgSO4 and concentration afforded 1.49 g of N-{2-[2-phenyl-5-(4-propyl-cyclohexyl)-pyrrol-1-yl]-acetyl}-guanidine as a yellow-brown oil. The product was observed to contain DMF by 1H NMR. However, it was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488832B2
Source datasetuspto-grants-2009_02
ORD IDord-f50e165767a5413780ba2f1102572433
Source noteuspto-grants-2009_02