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HRID 54851作成日:2026年10月24日

2-(2-Aminoethyl)benzimidazole dihydrochloride → Tricyclo[3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(1H-benzimidazol-2-yl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamate

https://huagongshe.com/ja/reaction/54851

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2-Aminoethyl)benzimidazole dihydrochlorideHCID 2788071—
反応物2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophanHCID 14802503—
溶媒TriethylamineHCID 8471—
生成物Tricyclo[3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(1H-benzimidazol-2-yl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamateHCID 86747494—

反応手順

Following the procedure of Example 70, the title compound was prepared from 0.50 g (1.26 mmol) of 2-adamantyloxycarbonyl-α-methyl-DL-tryptophan and 0.33 g (1.41 mmol) of 1H-benzimidazole-2-ethanamine dihydrochloride with 0.5 mL of added triethylamine. The purified product after chromatography was obtained as a white foam, 0.38 g (56%); 1H NMR (CDCl3) δ1.46-1.91 (17H, m), 3.01-3.16 (2H, m), 3.27 (1H, d, J 15 Hz), 3.43 (1H, d, J 15 Hz), 3.58 (2H, m), 4.80 (1H, br s), 5.23 (1H, s), 6.67 (1H, m), 6.89-7.72 (10H, m), 8.28 (1H, br s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622983
出典データセットuspto-grants-1997_04
ORD IDord-391b5d5066a74c0abd4cbb3d88442d64
出典メモuspto-grants-1997_04