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5-Cycloheptylmethyl-2-naphthalen-2-yl-1H-imidazole-4-carboxylic Acid → 5-Cycloheptylmethyl-2-naphthalen-2-yl-1H-imidazole-4-carboxylic Acid (3,5-bis-methoxycarbonyloxymethyl-phenyl)-amide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Cycloheptylmethyl-2-naphthalen-2-yl-1H-imidazole-4-carboxylic Acid | HCID 11559331 | — |
| 反応物 | Carbonic acid 3-amino-5-methoxycarbonyloxymethyl-benzyl ester methyl ester | HCID 18405533 | — |
| 生成物 | 5-Cycloheptylmethyl-2-naphthalen-2-yl-1H-imidazole-4-carboxylic Acid (3,5-bis-methoxycarbonyloxymethyl-phenyl)-amide | HCID 11621340 | 42% |
反応手順
5-Cycloheptylmethyl-2-naphthalen-2-yl-1H-imidazole-4-carboxylic acid (Example 20, step c) (605 mg, 1.75 mmol) was reacted with 3,5-bis-methoxycarbonyloxymethyl-aniline (492 mg, 1.75 mmol) according to the procedure of Example 20, step d to afford the product as a white solid (438 mg, 42%). 1H NMR (300 MHz, CDCl3) 9.42 (1H, br s), 9.35 (1H, s), 8.27 (1H, s), 8.06-7.89 (4H, m), 7.79 (2H, s), 7.56 (2H, m), 7.14 (1H, s), 5.18 (4H, s), 3.83 (6H, s), 3.12 (2H, d), 2.00-1.29 (13H, m).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06479531B1 |
| 出典データセット | uspto-grants-2002_11 |
| ORD ID | ord-63c8716bdf53448084f6e6c22590cce4 |
| 出典メモ | uspto-grants-2002_11 |