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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532696Generated: October 31, 2026

Docosanoic Acid → HCID 22013734, compound

https://huagongshe.com/reaction/1532696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDocosanoic AcidHCID 8215—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 22013746HCID 22013746—
SolventChloroformHCID 6212—
ProductHCID 22013734HCID 2201373461%

Reaction Steps

Triethylamine (1.52 ml) was added to a suspension containing n-docosanoic acid (3.339 g) in chloroform (34 ml), and then ethyl chlorocarbonate (1.04 ml) was added thereto while being cooled with ice. The reaction mixture was stirred for 1.5 hours, and then a solution containing 3-amino-4-{[2-(dimethylarnino)ethyl]amino}-N,N-dimethylbenzamide (2.454 g) in chloroform (12 ml) was added thereto. After being stirred for 3 hours while being cooled with ice, the reaction mixture was diluted with chloroform, washed with saturated sodium hydrogencarbonate aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (8.2 ml) was added to a suspension containing the residue (6.094 g) in ethanol (61 ml). After being stirred for 1.5 hours at 90° C., the reaction mixture was concentrated. The residue, with ethyl acetate added thereto, was washed with 1N sodium hydroxide aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The residue (5.119 g) was purified by silica gel column chromatography (silica gel 100 g, chloroform:methanol=50:1-30:1), thereby yielding the entitled compound (3.320 g) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-59e0efafa9134bc593512a74d9b03a99
Source noteuspto-grants-2001_03