HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Chloro-4-methylpyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Chloro-4-methylpyridine-3-carboxylic acid | HCID 15483766 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloro-4-methylpyridine-3-carboxamide | HCID 10942886 | 91% |
Reaction Steps
To a mixture of 2-chloro-4-methyl-3-pyridinecarboxylic acid (24.7 g, 157 mmol) and 75 mL of toluene at 70° C. was added 75 mL of SOCl2 (22.6 g, 190 mmol) within a period of 1 hour. The reaction mixture was refluxed for 4 hours and the resulting solution was cooled to room temperature. Dry NH3 gas was introduced at such a rate so as to maintain the internal temperature below 30° C. After removing toluene, the solid residue was washed successively with cold water and methanol, and dried to yield 22.72 g of the title compound (91%, m.p. 168°-170° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05493028 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-7153c737860b4ca2803911bb6ce5a8eb |
| Source note | uspto-grants-1996_02 |