関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Ethyl orthoformate | HCID 31214 | — |
| 反応物 | 2-Aminoindane | HCID 76310 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 2-Amino-3-cyanofuran | HCID 22719613 | — |
| 生成物 | 4-(2-Indanylamino)furo[2,3-d]pyrimidine | HCID 22719599 | 7.2% |
反応手順
A mixture of 2-amino-3-cyanofuran (270 mg, 2.5 mmol), triethyl orthoformate (1.5 ml, 9.0 mmol), and acetic anhydride (0.18 ml, 1.9 mmol) was heated to reflux at 130° C. for 2 hours. The reaction mixture was cooled, and 2-aminoindan (670 mg, 5.0 mmol), sodium acetate (640 mg, 7.8 mmol), and acetic acid (1.1 ml, 19 mmol) were added, which was further heated to reflux at 130° C. for 2 hours. The residue obtained by distilling off the solvent under reduced pressure was purified by silica gel chromatography (hexane:ethyl acetate=2:1) to obtain the title compound (44 mg, 0.18 mmol) having the following physical properties:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06703421B1 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-024ce929433f44509d6cf287f724db6b |
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| 出典メモ | uspto-grants-2004_03 |
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