HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916807Generated: October 30, 2026
HCID 69386463, compound → HCID 69385147, compound
https://huagongshe.com/reaction/916807
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 69386463 | HCID 69386463 | — |
| Reactant | HCID 178504318 | HCID 178504318 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ammonia methanol | HCID 21705897 | — |
| Product | HCID 69385147 | HCID 69385147 | 68.2% |
Reaction Steps
3-{[2-(4-{2-[(5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]ethyl}phenoxy)ethoxy]methyl}benzonitrile (125 mg) in THF (3 mL) was treated with KOSiMe3 (152 mg) and the resulting solution was heated at 75° C. for 4 h. The reaction mixture was then quenched with MeOH and concentrated in vacuo. The residue was taken up in EtOAc, washed with phosphate buffer (pH=6.5) and water, dried (MgSO4) and concentrated in vacuo. The residue was purified by chromatography (SPE, 5 g) eluting with CH2Cl2-MeOH-2M NH3 in MeOH (196:3:1) and then CH2Cl2: MeOH: 2M NH3/MeOH (96:3:1) to give the title compound (42 mg). LCMS RT=2.40 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07271197B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-48b7fbaa51fe46b480f156c54f811227 |
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| Source note | uspto-grants-2007_09 |
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