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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766371Generated: November 3, 2026

Triethylamine → HCID 21110118, compound

https://huagongshe.com/reaction/1766371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetylethanolamineHCID 8880—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 21110134HCID 21110134—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21110118HCID 21110118—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 40 mg (0.1 mmol) of the compound of Example 47 in 0.3 ml dry dimethylformamide are added 48.6 mg (0.3 mmol) N,N-carbonyldiimidazole. After allowing the reaction mixture to stand for one hour, the reaction mixture is diluted with water and extracted with ethyl acetate. After drying with magnesium sulfate, the solvent is evaporated off in vacuo. To the residue are added 0.5 ml (560 mg, 5.44 mmol) N-2-hydroxyethyl-acetamide and 10 μl (0.07 mmol) triethylamine. The reaction mixture is stirred at 100° C. for one hour. Then the reaction mixture is filtered and purified by preparative HPLC (column: Nucleosil 100-5 C 18 Nautilus 20 mm×50 mm, 5 μm; solvent A: acetonitrile, solvent B: water+0.1% formic acid; gradient: 0 min 10% A, 2 min 10% A, 6 min 90% A, 7 min 90% A, 7.1 min 10% A, 8 min 10% A; wavelength: 220 nm; injection volume: approx. 550 μl; number of injections: 1). The product containing fractions are combined and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230017B2
Source datasetuspto-grants-2007_06
ORD IDord-93e76f052ea7473bb8b8e448ffc281ce
Source noteuspto-grants-2007_06