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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897150Generated: October 29, 2026

Trifluoroacetic acid → [(+)-2-(4-{2-[6-(methylamino)pyridin-2-yl]ethoxy}phenyl)cyclopropyl]Acetic Acid Trifluoroacetate

https://huagongshe.com/reaction/897150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2-[6-(Methylamino)-2-pyridyl]ethan-1-olHCID 10534858—
ReactantEthyl [(+)-2-(4-hydroxyphenyl)cyclopropyl]acetateHCID 11298964—
SolventTetrahydrofuranHCID 8028—
Product[(+)-2-(4-{2-[6-(methylamino)pyridin-2-yl]ethoxy}phenyl)cyclopropyl]Acetic Acid TrifluoroacetateHCID 6974344215%

Reaction Steps

To a solution of 2-[6-(methylamino)pyridin-2-yl]ethanol (1 g, 6.6 mmol) and PPh3 polymer bound (1.4 g, 9.9 mmole) in dry THF (50 mL) was added ethyl [(+)-2-(4-hydroxyphenyl)cyclopropyl]acetate (1.4 g, 6.6 mmol) from example 1 step 1, followed by diisopropyl azodicarboxylate (1.5 ml, 7.7 mmol). The reaction mixture was stirred at room temperature. After 18 hours, PPh3 polymer was filtered through celite and washed with excess THF. Filtrate was concentrated. The concentrated residue was dissolved in 1:1/acetonitrile:water (40 ml) and treated with LiOH (1 g). Reaction was heated two hours at 55° C. then cooled to room temperature. Reaction was acidified by adding TFA and purified on reverse phase HPLC twice to give 0.45 g (15%) of title compound. 1H NMR (400 MHz, CD3OD) δ 7.8 (m, 1 H), 7.0 (d, 2 H, J=8.6 Hz), 6.9-6.6 (m, 4 H), 4.26 (t, 2 H, J=6 Hz), 3.21 (t, 2 H, J=6 Hz), 3.0 (s, 3 H), 2.35-2.33 (m, 2 H), 1.71-1.67 (m, 1 H), 1.21-1.18 (m, 1 H), 0.89-0.76 (m, 2 H). HRMS calcd for C19H22N2O3 (M+H): 327.1703. found 327.1677.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921767B2
Source datasetuspto-grants-2005_07
ORD IDord-a268ae0c04ba47c6bea61bc9f15673d1
Source noteuspto-grants-2005_07