HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzonitrile → HCID 178462395, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 178497886 | HCID 178497886 | — |
| Product | HCID 178462395 | HCID 178462395 | 75% |
Reaction Steps
In the same manner as that described in Example 3(4) a reaction was carried out using commercially available 4-aminobenzonitrile (98 mg, 0.83,mmol), trimethylaluminium (0.78 ml, 1.07M n-hexane solution, 0.83 mmol) and methyl 4-[trans-5-[[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]thio]-1,3-dioxan-2-yl]-3-fluorobenzoate (109 mg, 0.21 mmol) obtained in Example 5(2) and the reaction mixture was treated using a similar procedure to that described in Example 3(4) to give the title compound (95 mg, yield 75%) as a colorless oil which was recrystallized from ethyl acetate-hexane to give white powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06653330B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-d2acf36c55e844f4ad4cacb3b4c6f39b |
| Source note | uspto-grants-2003_11 |