HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202962Generated: November 1, 2026
4-Methylbenzyl alcohol → HCID 89702547, compound
https://huagongshe.com/reaction/2202962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzyl alcohol | HCID 11505 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | 1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)-4-hydroxypyridin-2(1H)-one | HCID 89691084 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89702547 | HCID 89702547 | 21.5% |
Reaction Steps
To a solution of 1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)-4-hydroxypyridin-2(1H)-one (170 mg), (4-methylphenyl)methanol (148 mg) and tributylphosphine (454 μl) in THF (15 ml) was added 1,1′-(azodicarbonyl)dipiperidine (458 mg). The mixture was stirred under sonication at 60° C. for 4 h. The reaction mixture was then cooled to room temperature, and concentrated in vacuo. The residue was diluted with DCM, washed with water and brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (MeOH/DCM) to give the title compound (50 mg) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365540B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-442d63afbf99427391ed76f028723ce6 |
|---|
| Source note | uspto-grants-2016_06 |
|---|