関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Triphenylcarbinol | HCID 6457 | — |
| 反応物 | HCID 19036273 | HCID 19036273 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 178468945 | HCID 178468945 | 107.9% |
反応手順
A mixture of 300 mg of ethyl 4-(1-hydroxy-1-methylethyl)-2-methylthiomethyl-1-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylate [prepared as described in step (d) above] and 5 ml of a 25% v/v aqueous solution of acetic acid was stirred at 60° C. for 1 hour. At the end of this time, the resulting solution was mixed with 5 ml of water and cooled with ice. The trityl alcohol which appeared as crystals was filtered off, and the filtrate was concentrated by evaporation under reduced pressure. Acetic acid and water in the residue were removed by distillation as azeotropic mixtures with toluene, to give 217 mg of the title compound as an amorphous powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05616599 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-6a8bff4ecc534fbebdd8ba62423bc5b9 |
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| 出典メモ | uspto-grants-1997_04 |
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