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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158108Generated: October 26, 2026

Triethylamine → HCID 178453727, compound

https://huagongshe.com/reaction/1158108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-(2-((tert-Butoxycarbonyl)amino)ethoxy)benzoic acidHCID 2755997—
ReactantHCID 178422083HCID 178422083—
SolventDichloromethaneHCID 6344—
ProductHCID 178453727HCID 178453727412.1%

Reaction Steps

A mixture of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (534 mg, 1.66 mmol), 4-[2-(Boc-amino)ethyloxy]-benzoic acid (NeoMPS, 701 mg, 2.49 mmol), EDCI (Aldrich, 637 mg, 3.32 mmol, 2.0 eq), HOBt (Aldrich, 45 mg, 0.332 mmol, 0.2 eq) and triethylamine (Aldrich, 336 mg, 3.32 mmol, 2.0 eq) in CH2Cl2 (10 mL) was stirred at room temperature for ca. 18 h. The reaction was quenched with saturated NaHCO3 (100 mL), and the crude product was extracted with CH2Cl2 (3×100 mL). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. Flash column chromatography (silica gel, 0-5% MeOH in CH2Cl2) afforded the title compound as a white solid (800 mg). MS (ESI, pos. ion) m/z: 585 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807700B2
Source datasetuspto-grants-2010_10
ORD IDord-bbb4a65ec49d41fd99fb995156ae6844
Source noteuspto-grants-2010_10