Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 19036248 | HCID 19036248 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178440143 | HCID 178440143 | 99.3% |
Reaction Steps
A suspension of 1.65 g of 4-(1-hydroxy-2,2-dimethylpropyl)-2-propyl-1-{4-[2-(trityltetrazol-5-yl)phenyl]-phenyl}methylimidazole-5-carbonitrile [prepared as described in step (b) above] in 24 ml of 75% v/v aqueous acetic acid was stirred at 60° C. for 2 hours. At the end of this time, 6 ml of water was added to the reaction mixture, which was then cooled with ice. The trityl alcohol which precipitated was removed by filtration, and the filtrate was concentrated by evaporation under reduced pressure, to give 1.07 g of the title compound as a glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646171 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-4afbaebd24394651b151e1a052829962 |
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| Source note | uspto-grants-1997_07 |
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