関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Oxalic Acid | HCID 971 | — |
| 反応物 | Oxalic acid dihydrate | HCID 61373 | — |
| 反応物 | N-[[2'-(1-Triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]valine methyl ester | HCID 11399301 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 溶媒 | 1-Propanol | HCID 1031 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Isobutanol | HCID 6560 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-[[2'-(1-Triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]valine methyl ester | HCID 11399301 | — |
| 生成物 | N-[[2'-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]valine methyl ester oxalate | HCID 23725720 | — |
反応手順
N-[[2′-(1-Triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]valine methyl ester (X) is prepared according to the process described in U.S. Pat. No. 5,399,578. N-[[2′-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]valine methyl ester (X) is reacted with a molar equivalent of oxalic acid or its hydrates selected from oxalic acid dihydrate in an organic solvent selected from alcohols such as ethanol, n-propanol, isopropanol, n-butanol, isobutanol, methylene chloride, ethyl acetate or mixtures thereof, at a temperature of about −20° C. to about 70° C. and the product obtained is isolated by filtration and dried. The product obtained is purified in a solvent selected from chlorinated hydrocarbons such as methylene chloride, chloroform, 1,2-dichloroethane, preferably methylene chloride to produce N-[[2′-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]valine methyl ester oxalate (Xa) in crystalline form. It has been observed that preparation of oxalic acid salt of Formula (X) results in greater than 98% purity of product by HPLC analysis.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07880015B2 |
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| 出典データセット | uspto-grants-2011_02 |
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| ORD ID | ord-f0c91159fd7f419f9b1c4b6f0def4e40 |
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| 出典メモ | uspto-grants-2011_02 |
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