Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-Amino-5-nitropyridine | HCID 77888 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 2933534 | HCID 2933534 | 83.9% |
Reaction Steps
P-toluenesulfonyl chloride (143.9 g) was added to a pyridine solution (800 mL) of 2-amino-5-nitropyridine (100 g), and stirred overnight at 110° C. The reaction solution was poured into water with ice, and stirred at 15° C. or lower for 30 minutes. The precipitate was taken out through filtration, and the resulting residue was washed with water, diethyl ether (1500 mL) and ethyl acetate (1000 mL), and dried under reduced pressure to obtain the entitled compound (176.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566781B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-8022163897b3450b8dc4c8bb564958e7 |
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| Source note | uspto-grants-2009_07 |
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