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Acetic acid, 2-(4-formylphenoxy)- → Pyrimidin-2,4-dione, 6-amino-5-[(4-carboxymethoxy)benzimidoyl]-1,3-dipr
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic acid, 2-(4-formylphenoxy)- | HCID 89177 | — |
| 反応物 | 5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione | HCID 5098605 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Pyrimidin-2,4-dione, 6-amino-5-[(4-carboxymethoxy)benzimidoyl]-1,3-dipr | HCID 614654 | — |
反応手順
A representative synthesis of benzylidene adduct is given. Compound A (1.51 g, 8.37 mmol) was dissolved in a mixture of methanol (35 ml) and acetic acid (5 ml) in a 50 ml boiling flask on a steam bath. To this was added a methanolic solution (60 ml) of freshly synthesized 5,6-diamino-1,3-dipropyluracil. After heating 15 minutes, the volume was reduced by evaporation until crystallization occurred. Ether (40 ml) was added and the nearly white solid was collected. Yield 2.80 g (86%), mp 179°-180° C. Analysis (C19H24N4O5): calc. 58.60% C, 6.21% H, 14.39% N; found 58.72% C, 6.16% H, 14.43% N.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04612315 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-a7d385ad8eba4da9bf9d492fd1a5c7a1 |
| 出典メモ | uspto-grants-1986_09 |