HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoro-3-(trifluoromethyl)aniline → HCID 178422778, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoro-3-(trifluoromethyl)aniline | HCID 75377 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 178496992 | HCID 178496992 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178422778 | HCID 178422778 | 35.3% |
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), 4-fluoro-3-(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 0.048 g of the desired product. 1HNMR (DMSO-d6): δ 1.57 (s, 6H), 3.06 (s, 2H), 7.24 (s, 1H), 7.51 (t, J=9.6 Hz, 1H), 7.84 (m, 1H), 8.30 (d, J=4.2 Hz, 1H), 8.45 (s, 2H), 9.84 (s, 1H), 11.99 (br s, 1H), 11.53 (br s, 1H); MS [M+H]+: 554.54.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08519149B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a172c04c81c24ff7877e9d5864d4fa05 |
| Source note | uspto-grants-2013_08 |