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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060242Generated: November 2, 2026

Triethylamine → [[2-(acetylamino)-5-thiazolyl]thio]-N-(2-oxobutyl)acetamide

https://huagongshe.com/reaction/1060242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant[[2-(Acetylamino)-5-thiazolyl]thio]acetic acidHCID 5329677—
Reactant1-aminobutan-2-one HydrochlorideHCID 11607912—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[[2-(acetylamino)-5-thiazolyl]thio]-N-(2-oxobutyl)acetamideHCID 1094655190%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of [[2-(acetylamino)-5-thiazolyl]thio]acetic acid (9.0 g, 38.8 mmol), HOBT (5.94 g, 38.8 mmol) and ethyldimethylaminopropylcarbodiimide hydrochloride salt (11.16 g, 58.2 mmol) in DMF (50 mL) was stirred at 0° C. for 0.5 h. To this mixture was added 1-amino-2-butanone hydrochloride (5.27 g, 42.7 mmol) followed by triethylamine (15 mL, 107.5 mmol). The mixture was stirred at 0° C. for 0.5 h and at rt for 1 h. Water (200 mL) was added to the mixture and the product was extracted with methylene chloride containing 10% MeOH (5×100 mL). The methylene chloride extract was dried over Na2SO4 and concentrated. The residue was triturated with water and the precipitated solid product was collected by filtration. It was dried to obtain the desired product (10.5 g, 90%), mp 195-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521759B2
Source datasetuspto-grants-2003_02
ORD IDord-6b00cbfc7d054a349ada2e99df01a9ca
Source noteuspto-grants-2003_02