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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532664Generated: October 30, 2026

Stearoyl chloride → HCID 9871822, compound

https://huagongshe.com/reaction/1532664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearoyl chlorideHCID 8212—
ReactantTriethylamineHCID 8471—
Reactant3-Amino-4-[[3-(dimethylamino)propyl]amino]-N-methylbenzamideHCID 22013751—
SolventChloroformHCID 6212—
ProductHCID 9871822HCID 987182284.9%

Reaction Steps

Triethylamine (0.77 ml) was added to a solution containing 3-amino-4-{[3-(dimethylamino)propyl]amino}-N-methylbenzamide (1.44 g) in chloroform (10 ml), and then a solution containing stearoyl chloride (1.51 g) in chloroform (5 ml) was added thereto while being cooled with ice. After being stirred for 1.5 hours at room temperature, the reaction mixture was diluted with chlorofonr, washed with saturated sodium hydrogencarbonate aqueous solution and water successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (4.00 ml) was added to a solution containing the residue (2.78 g) in ethanol (25 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 4N sodium hydroxide aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The residue (2.77 g) was purified by silica gel column chromatography (silica gel 50 g, chloroform:methanol=50:1-10:1), thereby yielding the entitled compound (2.11 g) as grayish yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-695e53c7227246ce9483aedf4ad050a3
Source noteuspto-grants-2001_03