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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393760Generated: October 26, 2026

P-Xylene → 2-(5-Nitrothiophen-2-yl)oxazolo[5,4-c]pyridine

https://huagongshe.com/reaction/1393760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantN-(3-hydroxypyridin-4-yl)-5-nitrothiophene-2-carboxamideHCID 59680090—
SolventPyridineHCID 1049—
Product2-(5-Nitrothiophen-2-yl)oxazolo[5,4-c]pyridineHCID 5967993217.2%

Reaction Conditions

Temperature160 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345178B2
Source datasetuspto-grants-2008_03
ORD IDord-8756dbc0a405497fabfec09c5d0cb11b
Source noteuspto-grants-2008_03