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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724333Generated: October 25, 2026

Triethylamine → HCID 178477280, compound

https://huagongshe.com/reaction/724333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-(4-amino-cyclohexyl)-3-hydroxy-2,2-dimethyl-propionamide hydrochlorideHCID 21877127—
Reactant2-[3-(Ethylsulfanyl)phenoxy]-5-fluoronicotinic acidHCID 21877135—
SolventDimethylformamideHCID 6228—
ProductHCID 178477280HCID 178477280—

Reaction Steps

2-(3-Ethylsulfanyl-phenoxy)-5-fluoro-nicotinic acid (150 mg, 0.51 mmol) was added to a solution of N-(4-amino-cyclohexyl)-3-hydroxy-2,2-dimethyl-propionamide hydrochloride (80:20 cis:trans, 135 mg, 0.54 mmol) and triethylamine (0.21 ml, 1.5 mmol) in dimethylformamide (3 ml) under nitrogen at room temperature. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (108 mg, 0.56 mmol) followed by 1-hydroxybenzotriazole (76 mg, 0.56 mmol) were then added and the reaction was stirred at room temperature for 20 h. The mixture was concentrated under reduced pressure, partitioned between ethyl acetate (20 ml) and water (20 ml) and the organic phase was removed, dried over MgSO4 and concentrated under reduced pressure. The residue was purified by flash column chromatography on a silica gel eluting with a solvent gradient of dichloromethane:methanol (95:5) and the product was purified by preparative HPLC to give two products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141586B2
Source datasetuspto-grants-2006_11
ORD IDord-6bf41a25e3d7400ea611bc57bfaeceee
Source noteuspto-grants-2006_11