HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-Methylamino-5-nitro-2-(4-trifluoromethyl-piperidinyl)-nicotinic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-(Trifluoromethyl)piperidine | HCID 136469 | — |
| Reactant | 2-(2,2-Difluoro-ethoxy)-6-methylamino-5-nitro-nicotinic acid | HCID 86669291 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Methylamino-5-nitro-2-(4-trifluoromethyl-piperidinyl)-nicotinic acid | HCID 67958409 | — |
Reaction Steps
A mixture of 4-trifluoromethyl-piperidine (330 mg, 2.2 mmol), TEA (1.00 mL, 7.2 mmol), 2-(2,2-difluoro-ethoxy)-6-methylamino-5-nitro-nicotinic acid (500 mg, 1.8 mmol, prepared according to WO2010/34799), DMF (5 mL) and MeCN (5 mL) is stirred for 3 h at rt. Then Cs2CO3 (1.5 g, 4.6 mmol) is added and it is stirred overnight at rt and for 6 h at 70° C. Water is added and the mixture is concentrated i.vac. The residue is diluted with water, HCOOH is added and the resulting precipitate is filtered, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486968B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-c82ba926a9e74a0ea90cf87315144d7f |
| Source note | uspto-grants-2013_07 |