Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 86749044 | HCID 86749044 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178440072 | HCID 178440072 | 58.5% |
Reaction Steps
1.5 ml of water were added to a solution of 527 mg of methyl {4'-[4-(1-hydroxy-1-methylethyl)-2-propyl-5-(2-trityltetrazol-5-yl)imidazol-1-ylmethyl]biphenyl-2-yl}glyoxylate [prepared as described in step (a) above] dissolved in 3.5 ml of acetic acid, and the resulting mixture was stirred at 70° C. for 1.5 hours. At the end of this time, 2 ml of water were added to the mixture. The resulting mixture was ice-cooled, and then the precipitate was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residual acetic acid was removed by azeotropic distillation with toluene, to give 206 mg of the title compound, as crystals melting at 131°-132° C. (after crystallization from a mixture of diethyl ether and ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05459148 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-aa3b54799f48483fad12b7bf6ae9f9d8 |
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| Source note | uspto-grants-1995_10 |
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