HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389746Generated: October 27, 2026
Stannane, hydroxytrimethyl- → 2-(2,6-Difluorophenyl)-5-(phenylamino)oxazole-4-carboxylic acid
https://huagongshe.com/reaction/389746
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannane, hydroxytrimethyl- | HCID 11217597 | — |
| Reactant | Ethyl 2-(2,6-difluorophenyl)-5-(phenylamino)oxazole-4-carboxylate | HCID 59587399 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2,6-Difluorophenyl)-5-(phenylamino)oxazole-4-carboxylic acid | HCID 59587543 | 41.3% |
Reaction Steps
To a solution of ethyl 2-(2,6-difluorophenyl)-5-(phenylamino)oxazole-4-carboxylate (0.080 g, 0.23 mmol) in DCE (8 mL) was added trimethyltin hydroxide (0.300 g, 1.66 mmol) and the resulting solution stirred at 80° C. overnight. A further portion of trimethyltin hydroxide (0.168 g, 0.93 mmol) was added and the solution stirred at 80° C. overnight. The reaction was diluted with DCM and washed with 1M aqueous HCl and brine. The organic phase was dried over MgSO4 and solvent removed in vacuo. The residue was purified by silica gel column chromatography using an 8% to 50% EtOAc in hexanes gradient followed by a 5% to 50% MeOH in DCM gradient to afford 2-(2,6-difluorophenyl)-5-(phenylamino)oxazole-4-carboxylic acid (0.030 g, 0.095 mmol, 41% three steps). LCMS (1) Rt: 1.46 min; m/z (ES+) 317.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378095B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-0e80ec1c7f544c14b77a1facd41a8dc8 |
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| Source note | uspto-grants-2013_02 |
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