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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410407Generated: November 1, 2026

Tetrahydrofuran → (2S,3R)-3-(formyloxy)-2-[2-(4-oxo-1,2,3-benzotriazin-3(4H)-yl)ethyl]-5-(4-pyrimidin-5-ylphenyl)pentanoic acid

https://huagongshe.com/reaction/2410407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium PermanganateHCID 516875—
ReactantSodium periodateHCID 23667635—
ReactantHCID 67184114HCID 67184114—
Solventtert-ButanolHCID 6386—
Product(2S,3R)-3-(formyloxy)-2-[2-(4-oxo-1,2,3-benzotriazin-3(4H)-yl)ethyl]-5-(4-pyrimidin-5-ylphenyl)pentanoic acidHCID 86700967—

Reaction Steps

To a solution of the compound obtained from step m above (0.25 g) in tert-butanol: tetrahydrofuran (5 mL:5 mL) at 0° C., a solution of sodium metaperiodate (0.465 g in 5 mL of water) was added. The reaction mixture was stirred for 2 hours at the same temperature and potassium permanganate (0.017 g) was added at 0° C. After stirring the reaction mixture for an additional 6 hours at room temperature, the reaction mixture was evaporated on a rotary evaporator. The residue was taken into water and extracted with ethyl acetate. The organic layer was washed with water and brine solution and dried over anhydrous sodium sulphate. The solvent was evaporated under the reduced pressure to afford the title compound (0.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816073B2
Source datasetuspto-grants-2014_08
ORD IDord-5a317c3ea1b44f0f9fe7a2560034f9a9
Source noteuspto-grants-2014_08