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HRID 1018310作成日:2026年10月25日

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

https://huagongshe.com/reaction/1018310

反応式

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 AcidHCID 11559331—
反応物Carbonic acid 3-amino-5-methoxycarbonyloxymethyl-benzyl ester methyl esterHCID 18405533—
生成物5-Cycloheptylmethyl-2-naphthalen-2-yl-1H-imidazole-4-carboxylic Acid (3,5-bis-methoxycarbonyloxymethyl-phenyl)-amideHCID 1162134042%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479531B1
出典データセットuspto-grants-2002_11
ORD IDord-63c8716bdf53448084f6e6c22590cce4
出典メモuspto-grants-2002_11