HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzonitrile → HCID 178462390, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 178497759 | HCID 178497759 | — |
| Product | HCID 178462390 | HCID 178462390 | 94.4% |
Reaction Steps
In the same manner as that described in Example 3(4) a reaction was carried out using commercially available 4-aminobenzonitrile (138 mg, 1.2 mmol), trimethylaluminium (1.08 ml, 1.07M n-hexane solution, 1.2 mmol) and methyl 3-[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]benzoate (147 mg, 0.29 mmol), obtained in Example 6(1), and the reaction mixture was treated using a similar procedure to that described in Example 3(4) to afford the title compound (162 mg, yield 94%) as a pale yellow oil which was recrystallized from ethyl acetate-hexane to give pale yellow powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06653330B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-10b0d07a178a4efc9b6cb5e69dcbdf52 |
| Source note | uspto-grants-2003_11 |