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HRID 1470514作成日:2026年10月27日
Oxalic Acid → 1-methyl-2[N-[4-amidinophenyl]aminomethyl]benzimidazol-5-yl-carboxylicacid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide oxalate
https://huagongshe.com/reaction/1470514
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Oxalic Acid | HCID 971 | — |
| 反応物 | Dabigatran Ethyl Ester | HCID 446804 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-methyl-2[N-[4-amidinophenyl]aminomethyl]benzimidazol-5-yl-carboxylicacid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide oxalate | HCID 57389347 | — |
反応手順
A mixture of 1-methyl-2-[N-[4-amidinophenyl]aminomethyl]benzimidazol-5-yl-carboxylicacid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide compound of formula-5 (100 g) and ethanol (1200 ml) was heated to 50-60° C. A solution of oxalic acid (25.25 g) in ethanol (1500 ml) was added to the above reaction mixture at 50-60° C. and stirred for 45 minutes. The reaction mixture was cooled to 25-35° C. and stirred for 6 hours at 25-35° C. Filtered the solid, washed with ethanol and then dried to get the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09006448B2 |
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| 出典データセット | uspto-grants-2015_04 |
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| ORD ID | ord-d548663fb9c64f02b3ede67f1688ca4a |
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| 出典メモ | uspto-grants-2015_04 |
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