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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517000Generated: October 25, 2026

p-Methylphenoxyacetic acid → 2-(4-Methylphenoxy)-1-(4-naphthalen-2-ylsulfonylpiperazin-1-yl)ethanone

https://huagongshe.com/reaction/517000

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Methylphenoxyacetic acidHCID 70329—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-1-[4-(naphthalene-2-sulfonyl)piperazin-1-yl]ethan-1-oneHCID 2405875—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
Product2-(4-Methylphenoxy)-1-(4-naphthalen-2-ylsulfonylpiperazin-1-yl)ethanoneHCID 115152777.5%

Reaction Steps

To a stirred solution of 2-chloro-1-(4-(naphthalen-2-ylsulfonyl)piperazin-1-yl)ethanone (compound 4, 0.2 g, 0.64 mmol) and 2-(p-tolyloxy)acetic acid (106 mg, 0.64 mmol) in dry DCM (20 mL), DIPEA (495 mg, 3.86 mmol) followed by HATU (486 mg, 1.27 mmol) was added at room temperature and stirred overnight. The mixture was then diluted with DCM and washed with water (2×10 mL) & brine (2×10 mL). The organic extract was dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure. The crude material was purified by column chromatography to yield the title compound (0.21 g, 77.5%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115086B2
Source datasetuspto-grants-2015_08
ORD IDord-31e27bbf07fe4a6c83d2dc5203b23350
Source noteuspto-grants-2015_08