HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-ethoxy-1-(ethoxymethyl)ethyl 2-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1h-imidazole-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 1,3-Diethoxy-2-propanol | HCID 77664 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Demiditraz | HCID 24738933 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-ethoxy-1-(ethoxymethyl)ethyl 2-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1h-imidazole-1-carboxylate | HCID 57718381 | — |
Reaction Steps
To a mixture of Example 58 (500 mg, 2.5 mmol) and pyridine (0.44 ml, 5.5 mmol) in anhydrous dichloromethane (5 ml), at 0° C. and under nitrogen, was added phosgene (20% in toluene, 1.44 ml, 2.75 mmol). The mixture was stirred at 0° C. for 20 min, before addition of 1,3-diethoxypropan-2-ol (407 mg, 2.75 mmol). The reaction mixture was stirred at room temperature for 30 min and then poured into ice water (10 ml). The mixture was adjusted to pH 7 by addition of solid sodium hydrogen carbonate and the two layers were separated. The aqueous phase was extracted with dichloromethane (2×10 ml) and the combined extracts were dried (MgSO4) and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592362B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-cb1b0eaa6ae84e558fab8c73622cbc7e |
| Source note | uspto-grants-2009_09 |