HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-[2-{1 [(2-chlorophenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}ethyl]phenylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-[2-{1-[(2 chlorophenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}ethyl]phenylalanine methyl ester | HCID 22847671 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[2-{1 [(2-chlorophenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}ethyl]phenylalanine | HCID 54198642 | — |
Reaction Steps
The procedure of Example 2 (ii) was followed using 0.9 g (1.99 mmol) of N-[2-{1-[(2-chlorophenyl)methyl]-2-n-butyl-1H-imidazol -5-yl}ethyl]phenylalanine methyl ester, 0.33 g of potassium hydroxide, 15 ml of water and 25 ml of ethanol to afford after workup 0.54 q of product. Trituration with ether provided the title compound; mp 78°-80° C. (free base) and mp 232°-233° C. (for the dihydrochloride salt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05248689 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-0938af2f3f7e40ac8becd6f17afdc7e9 |
| Source note | uspto-grants-1993_09 |