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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 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 acetate | HCID 68975033 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3R,4S)-4-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-1-(4-iodophenyl)azetidin-2-one | HCID 68977003 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622449B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-cae4dee2d06b43708f444f5f8b160279 |
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| Source note | uspto-grants-2009_11 |
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