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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85358Generated: October 28, 2026

Salicylic Acid → HCID 67175546, compound

https://huagongshe.com/reaction/85358

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), and 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 HCl, water, 5% NaHCO3 and water, and dried over MgSO4. The solvent was removed under reduced pressure. Purification of the crude product by preparative 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 numberUS08846972B2
Source datasetuspto-grants-2014_09
ORD IDord-a9b717fc59314d0c87542cdc586d2f28
Source noteuspto-grants-2014_09