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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708373Generated: October 30, 2026

Potassium Phosphate, Dibasic → Benzyl ((3S,4R)-2-oxo-4-((2-oxopyridin-1(2H)-yl)methyl)azetidin-3-yl)carbamate

https://huagongshe.com/reaction/708373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, DibasicHCID 24450—
ReactantBenzyl((3S,4R)-1-(2,4-dimethoxybenzyl)-2-oxo-4-((2-oxopyridin-1(2H)-yl)methyl)azetidin-3-yl)carbamateHCID 131733738—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductBenzyl ((3S,4R)-2-oxo-4-((2-oxopyridin-1(2H)-yl)methyl)azetidin-3-yl)carbamateHCID 13173373981%

Reaction Conditions

Temperature90 °C

Reaction Steps

Prepared in an analogous manner to example 4, step 2 using Benzyl ((3S,4R)-1-(2,4-dimethoxybenzyl)-2-oxo-4-((2-oxopyridin-1(2H)-yl)methyl)azetidin-3-yl)carbamate (361 mg, 0.622 mmol), K2S2O8 (225 mg, 0.833 mmol) and K2HPO4 (135 mg, 0.773 mmol) in ACN:water (2:1, 9.9 mL) while heating for 1.5 h at 90° C. More K2S2O8 (45 mg, 0.17 mmol) and K2HPO4 (26.9 mg, 0.155 mmol) were added and heated for another 30 min, whereupon it was concentrated, redissolved in EtOAc, washed with brine, dried over Na2SO4, and concentrated in vacuo. The crude residue was purified via silica gel chromatography (MeOH-DCM, 0-10%) to afford the title compound (157 mg, 81%). LCMS: Rt=0.56 min, m/z=328.2 (M+1) Method 2m_acidic.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-a6ded9f8fb2f42f2a0045da46a1d1c41
Source noteuspto-grants-2015_11