HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11382Generated: October 25, 2026
Sodium hydride → HCID 69279866, compound
https://huagongshe.com/reaction/11382
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Oxazole, 4-(chloromethyl)-2-(3,5-dimethoxyphenyl)-5-methyl- | HCID 21974252 | — |
| Reactant | Rac-2-ethoxy-3-(1h-indol-4-yl)-propionic acid ethyl ester | HCID 69279879 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69279866 | HCID 69279866 | 84% |
Reaction Steps
0.048 g (1.10 mmol) Sodium hydride (55% in mineral oil) was added in one portion below 5° C. and under argon to a stirred solution of 0.261 g (1.00 mmol) rac-2-ethoxy-3-(1H-indol-4-yl)-propionic acid ethyl ester and 0.321 g (1.20 mmol) 4-chloromethyl-2-(3,5-dimethoxy-phenyl)-5-methyl-oxazole in 15.0 ml N,N-dimethylformamide. The reaction mixture was warmed up to room temperature and then stirred for 16 hours at ambient temperature. It was then diluted with cold water and extracted two times with ethyl acetate. The combined organic phases were dried over MgSO4, filtered and evaporated. The residue formed was purified by flash-chromatography (silica gel; eluent: gradient of hexane and ethyl acetate) to give 0.413 g (84%) rac-3-{1-[2-(3,5-dimethoxy-phenyl)-5-methyl-oxazol-4-ylmethyl]-1H-indol-4-yl}-2-ethoxy-propionic acid ethyl ester as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098228B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-2bbd1173503f43e4a80adb2b4bc005c0 |
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| Source note | uspto-grants-2006_08 |
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