HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966935Generated: October 26, 2026
Potassium Carbonate → (4-Oxazol-5-yl-naphthalen-1-yl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/966935
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Toluene-sulfonylisocyanide | HCID 21875242 | — |
| Reactant | (4-Cyano-naphthalen-1-yl)-carbamic acid tert-butyl ester | HCID 58745930 | — |
| Reactant | tert-Butyl 4-formylnaphthalen-1-ylcarbamate | HCID 58745967 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-Oxazol-5-yl-naphthalen-1-yl)-carbamic acid tert-butyl ester | HCID 58745848 | 44% |
Reaction Steps
The above mixture of compounds 503A & 503B (3.37 g, 10.0 mmol; corrected for presence of compound 503A), toluene-sulfonylisocyanide (2.15 g, 11.0 mmol) and potassium carbonate (1.66 g, 12.0 mmol) in 50 mL of methanol was refluxed for 4 h. The reaction mixture was partitioned between water (200 mL) and chloroform (200 mL). After extracting the aqueous layer with chloroform (100 mL), the combined organic layers were dried over magnesium sulfate and concentrated in vacuo. The crude residue was purified by flash chromatography on silica gel eluting with a gradient of 10-40% ethyl acetate in hexane to give 1.35 g (44%) of compound 503C as a white solid. 1HNMR (400 MHz, DMSO-d6): δ 9.45 (s, 1H), 8.57 (s, 1H), 8.20 (m, 2H), 7.76 (m, 2H), 7.64 (s, 1H), 7.62 (m, 2H), 1.51 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953679B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-a3244177f8ab4cb782c0ec0c8935a529 |
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| Source note | uspto-grants-2005_10 |
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