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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053771Generated: October 30, 2026

Triethylamine → HCID 178427057, compound

https://huagongshe.com/reaction/2053771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-Methyl 4-(pyrrolidin-1-ylcarbonyl)benzoic acidHCID 12068686—
ReactantHCID 178463394HCID 178463394—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 178427057HCID 178427057—

Reaction Steps

A solution of 0.10 g (0.43 mmol) of 3-methyl-4-(pyrrolidin-1-ylcarbonyl)benzoic acid, 0.184 g (0.450 mmol) of 1-(5-fluoro-1H-benzimidazol-2-yl)ethylamine×2(CF3COOH) (prepared analogously to Methods 1a, 10b, 10c) and 0.35 mL (2.50 mmol) of triethylamine in 3 mL of dimethylsulfoxide is stirred at ambient temperature and combined with 0.193 g (0.600 mmol) of TBTU. The reaction mixture is stirred for 1 hour at ambient temperature, then diluted with ethyl acetate and washed successively with 10% aqueous citric acid, twice with 2 molar sodium hydroxide solution and with water. The organic phase is dried with sodium sulfate and concentrated. The crude product is taken up in ethyl acetate, precipitated with tert-butylmethylether, and dried. Yield: 83 mg (49% of theory); Rf value: 0.34 (silica gel; ethyl acetate/ethanol=9:1); C22H23FN4O2 (394.45); mass spectrum: (M+H)+=395

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326791B2
Source datasetuspto-grants-2008_02
ORD IDord-1f941352097c44439857730fad537154
Source noteuspto-grants-2008_02