Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-(2-Amino-5-nitropyridin-3-yl)-4-nitrobenzamide | HCID 58932933 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | HCID 178526539 | HCID 178526539 | 92.1% |
Reaction Steps
To a stirred suspension of N-(2-Amino-5-nitropyridin-3-yl)-4-nitrobenzamide (6) (1.15 g, 3.8 mmol) in ethylene glycol (75 mL) was added HCl (Conc., 3 drops) and the mixture heated at 160° C. for 6 h. The solution was cooled to room temperature and poured into H2O (200 mL) and the resulting solid collected by filtration, rinsed with H2O, and dried in vacuo at 80° C. to give 4 as a pale yellow solid (1 g, 3.5 mmol, 92%). 1H NMR (500 MHz, DMSO-d6) δ14.58 (br s, 1H), 9.28 (apparent d, 1H), 8.88 (br s, 1H), 8.51 (d, J=8.39 Hz, 2H), 8.45 (d, J=8.28 Hz, 2H). EIMS M−1 284.3. Rf=0.55 (silica, 19:1 DCM/MeOH)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256287B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-42f8341d2ef0491e9610628f78d092c0 |
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| Source note | uspto-grants-2007_08 |
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