HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene → 1-[3-(3,4-Difluoro-phenylamino)-5-(2-methyl-pyridin-4-yl)-[1,2,4]triazol-1-yl]-hexan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-1-[5-(2-Chloro-6-methyl-pyridin-4-yl)-3-(3,4-difluoro-phenylamino)-[1,2,4]triazol-1-yl]-butan-2-ol | HCID 86644737 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[3-(3,4-Difluoro-phenylamino)-5-(2-methyl-pyridin-4-yl)-[1,2,4]triazol-1-yl]-hexan-2-ol | HCID 59455888 | — |
Reaction Steps
A mixture of intermediate, 1-[5-(2-chloro-6-methyl-pyridin-4-yl)-3-(3,4-difluoro-phenylamino)-[1,2,4]triazol-1-yl]-hexan-2-ol (prepared according to D4) (1.5 g; 3.5 mmol) and Et3N (2 ml) in THF (40 ml) was hydrogenated with Pd/C 10% (0.020 g) as a catalyst in the presence of thiophene solution (0.1 ml; 4% in DIPE). After uptake of H2 (1 equiv) had ceased, the catalyst was filtered off and the filtrate was evaporated in vacuo. The residue was suspended in DIPE and filtrated. The crystals were dried in a vacuum oven at 70° C. overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440701B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-12adb2a7895f46cb9bb3ca04cbdcfd78 |
| Source note | uspto-grants-2013_05 |