HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,4-Difluoro-N-methyl-6-nitro-3-(4-trifluoromethyl-piperidin-1-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Trifluoromethyl)piperidine hydrochloride | HCID 16218160 | — |
| Reactant | 2,3,4-Trifluoro-N-methyl-6-nitroaniline | HCID 86674338 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,4-Difluoro-N-methyl-6-nitro-3-(4-trifluoromethyl-piperidin-1-yl)aniline | HCID 86674339 | — |
Reaction Steps
A mixture of 2,3,4-trifluoro-N-methyl-6-nitroaniline (1.5 g, 7.3 mmol), 4-trifluoromethyl-piperidine hydrochloride (2.76 g, 14.6 mmol), K2CO3 (2.01 g, 14.6 mmol) and DMF (10 mL) was stirred at rt overnight under Ar atmosphere. The mixture was poured into aqueous ammonia and extracted with EtOAc. The organic layer was dried over Na2SO4, filtered and concentrated. Crystallization from EtOAc/PE gave the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466186B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-dd2f917b2a064093ab63da8a2b75c3e1 |
| Source note | uspto-grants-2013_06 |