HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Acetic Acid 1-{4-[1-(4-cyclohex-1-enylphenyl)-3-(3,5-dichlorophenyl)ureidomethyl]-phenyl}-2-(2H-tetrazol-5-yl)ethyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(4-Cyclohex-1-enylphenyl)-3-(3,5-dichlorophenyl)-1-{4-[1-hydroxy-2-(2H-tetrazol-5-yl)ethyl]benzyl}urea | HCID 18768913 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetic Acid 1-{4-[1-(4-cyclohex-1-enylphenyl)-3-(3,5-dichlorophenyl)ureidomethyl]-phenyl}-2-(2H-tetrazol-5-yl)ethyl Ester | HCID 67482389 | — |
Reaction Steps
1-(4-Cyclohex-1-enylphenyl)-3-(3,5-dichlorophenyl)-1-{4-[1-hydroxy-2-(2H-tetrazol-5-yl)ethyl]benzyl}urea (30 mg, 0.05 mmol) was dissolved in DCM (1.5 ml) and acetic acid anhydride (15 μl) was added. The mixture was stirred at room temperature overnight, and then taken to dryness. The residual oil was dissolved in ethanol (2 ml), and heated to reflux for 0.5 min. Then cooled and evaporated to dryness. The residue was stripped twice from acetonitrile to give a quantitative yield of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06649641B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-0604f4a364804bf7aaa45016e8d83cb0 |
| Source note | uspto-grants-2003_11 |