HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-5-(trifluoromethyl)aniline → HCID 178422786, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-5-(trifluoromethyl)aniline | HCID 136349 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 178496992 | HCID 178496992 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178422786 | HCID 178422786 | 33.1% |
Reaction Steps
The title compound was prepared following the procedure described for Example-137 by using methyl 2-[(3,5-dichloropyridin-4-yl)amino]-7,7-dimethyl-7,8-dihydro-1H-furo[3,2-e]benzimidazole-5-carboxylate (Step-1 of Intermediate-3, 0.100 g, 0.245 mmol), 2-fluoro-5-(trifluoromethyl)aniline (0.064 g, 0.357 mmol), trimethyl aluminium (2M solution in toluene) (0.5 mL), dry toluene (5.0 mL) at room temperature to afford 0.045 g of the desired product. 1HNMR (DMSO-d6): δ 1.57 (s, 6H), 3.10 (s, 2H), 7.30 (s, 1H), 7.53-7.63 (m, 2H), 8.45 (s, 2H), 8.87 (d, J=6.6 Hz, 1H), 10.20 (s, 1H), 11.02 (br s, 1H), 11.59 (br s, 1H); MS [M+H]+: 551.97.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08519149B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-f36c51fdbc604ad5905570a8409c34f3 |
| Source note | uspto-grants-2013_08 |