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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437822Generated: October 25, 2026

Sodium Cyanide → (3R,4S)-4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-1-(4-iodophenyl)azetidin-2-one

https://huagongshe.com/reaction/1437822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant(1S)-3-[(2S,3R)-2-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-1-(4-iodophenyl)-4-oxoazetidin-3-yl]-1-(4-fluorophenyl)propyl acetateHCID 68975033—
SolventMethanolHCID 887—
Product(3R,4S)-4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-1-(4-iodophenyl)azetidin-2-oneHCID 68977003—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 15 mg (0.022 mmol) (1S)-3-[(2S,3R)-2-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-1-(4-iodophenyl)-4-oxoazetidin-3-yl]-1-(4-fluorophenyl)propyl acetate (Alternate Example 6, step A) in 1 mL anhydrous methanol under nitrogen atmosphere was added 2 mg of sodium cyanide. The reaction mixture was heated at 50° C. for 1.25 hr at which time the volatiles were removed by a nitrogen stream. The residue was purified by prep. Tlc eluting with EtOAc/hexanes (1/3) to afford the title compound. m/z (ES) 632.3 (MH+), 614.3 (MH−H2O+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622449B2
Source datasetuspto-grants-2009_11
ORD IDord-cae4dee2d06b43708f444f5f8b160279
Source noteuspto-grants-2009_11