HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419893Generated: October 27, 2026
P-Xylene → 2-(5-Nitrothiophen-2-yl)oxazolo[5,4-c]pyridine
https://huagongshe.com/reaction/419893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | N-(3-hydroxypyridin-4-yl)-5-nitrothiophene-2-carboxamide | HCID 59680090 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(5-Nitrothiophen-2-yl)oxazolo[5,4-c]pyridine | HCID 59679932 | 17.2% |
Reaction Steps
To a stirred solution of N-(3-hydroxypyridin-4-yl)-5-nitrothiophene-2-carboxamide (1.1 g, 4.1 mmol) in pyridine (5 mL) was added P2O5 (1.2 g, 8.3 mmol) and p-xylene (21 mL). After refluxing at 160° C. overnight, the reaction mixture was concentrated in vacuo and the residue was purified by chromatography on silica gel eluted with 5% of ethyl acetate in CH2Cl2 to give 2-(5-nitrothiophen-2-yl)oxazolo[5,4-c]pyridine as brown solid (174 mg, yield 17%). 1H NMR (400 MHz, CDCl3) δ: 8.97 (1H, s); 8.59 (1H, d, J=5.6); 7.94 (1H, d, J=4.4); 7.86 (1H, d, J=4.4), 7.69 (1H, d, J=5.6,0.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093401B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-eb7eed0b95864ad38256ac6172b4b41a |
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| Source note | uspto-grants-2012_01 |
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