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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922580Generated: October 31, 2026

Salicylic Acid → HCID 67175546, compound

https://huagongshe.com/reaction/1922580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylic AcidHCID 338—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 54312597HCID 54312597—
SolventAcetonitrileHCID 6342—
ProductHCID 67175546HCID 6717554619.7%

Reaction Steps

To a mixture of 1-(piperazin-1-yl)docosa-4,7,10,13,16,19-hexaen-1-one (1.17 g, 2.95 mmol), salicylic acid (0.61 g, 4.43 mmol) and Et3N (0.89 g, 8.85 mmol) in CH3CN (10 mL) was added HATU (1.68 g, 4.43 mmol). The mixture was stirred (RT, 16 h). The solvent was removed under reduced pressure and the residue was extracted with EtOAc (4×50 mL). The combined organic layers were washed successively with 1N aqueous HCl, water, 5% NaHCO3 and water, and dried over MgSO4. The solvent was removed under reduced pressure. Purification of the crude product by prep-HPLC afforded 1-(4-(2-hydroxybenzoyl)piperazin-1-yl)docosa-4,7,10,13,16,19-hexaen-1-one (300 mg, 19.6%) as a light yellow oil. Mass calculated for C33H44N2O3=516.71; found: [M+H]+ 517.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173831B2
Source datasetuspto-grants-2012_05
ORD IDord-33334afdceee48faa8ffc0c0ff1dc894
Source noteuspto-grants-2012_05