HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389327Generated: October 31, 2026
N,N,N',N'-Tetramethylazodicarboxamide → Ethyl[4-(2-{5-[bis(4-fluorophenyl)methyl]-2-oxopyridin-1(2h)-yl}ethoxy)-2-methyl-1h-benzimidazol-1-yl]acetate
https://huagongshe.com/reaction/2389327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylazodicarboxamide | HCID 4278 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 5-[Bis(4-fluorophenyl)methyl]-1-(2-hydroxyethyl)pyridin-2(1h)-one | HCID 68533594 | — |
| Reactant | ethyl (4-hydroxy-2-methyl-1H-benzimidazol-1-yl)acetate | HCID 86637909 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl[4-(2-{5-[bis(4-fluorophenyl)methyl]-2-oxopyridin-1(2h)-yl}ethoxy)-2-methyl-1h-benzimidazol-1-yl]acetate | HCID 131729955 | 94.4% |
Reaction Steps
To a mixture of ethyl (4-hydroxy-2-methyl-1H-benzimidazol-1-yl)acetate (476 mg), 5-[bis(4-fluorophenyl)methyl]-1-(2-hydroxyethyl)pyridin-2(1H)-one (694 mg), 1,1′-azobis(N,N-dimethylformamide) (385 mg) and toluene (9.5 mL) was added tributylphosphine (452 mg) at ambient temperature. The mixture was stirred at ambient temperature for 20 hours. The reaction mixture was diluted with a mixture of EtoAc (50 mL) and THF (20 mL), and washed with water (30 mL) and brine (30 mL). The organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo to give crude oil. The crude oil was crystallized from solvent(EtOAc and n-hexane) to give ethyl[4-(2-{5-[bis(4-fluorophenyl)methyl]-2-oxopyridin-1(2H)-yl}ethoxy)-2-methyl-1H-benzimidazol-1-yl]acetate (1.07 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273745B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-1929e57b2c1b460eb7c3ef091f5d99cd |
|---|
| Source note | uspto-grants-2012_09 |
|---|