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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335017Generated: October 29, 2026

Triethylamine → HCID 59464692, compound

https://huagongshe.com/reaction/335017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Chlorophenylacetic acidHCID 15879—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-(4-Nitrophenyl)-1-(2-thiophene-2-ylthiazol-4-yl)ethylamineHCID 66705334—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59464692HCID 5946469260%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(4-nitrophenyl)-1-(2-thiophene2-ylthiazol-4-yl)ethylamine, 22, (0.41 g, 1 mmol) 3-chlorophenylacetic acid (0.170 g, 1 mmol) and 1-hydroxybenzotriazole (HOBt) (0.070 g, 0.50 mmol) in DMF (5 mL) at 00, is added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDCI) (0.190 g, 1 mmol) followed by triethylamine (0.42 mL, 3 mmol). The mixture is stirred at 0° C. for 30 minutes then at room temperature overnight. The reaction mixture is diluted with water and extracted with EtOAc. The combined organic phase is washed with 1N aqueous HCl, 5% aqueous NaHCO3, water and brine, and dried over Na2SO4. The solvent is removed in vacuo to afford 0.290 g (60% yield) of the desired product which is used without further purification. ESI− MS 482 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883832B2
Source datasetuspto-grants-2014_11
ORD IDord-d755381b780c452694b8cf41ee9f7f6b
Source noteuspto-grants-2014_11