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HRID 54852作成日:2026年10月23日

2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophan → Tricyclo [3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(3,4-dihydro-1-naphthalenyl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamate

https://huagongshe.com/ja/reaction/54852

反応式

関与物質

役割名称HCID仕込み量
反応物2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophanHCID 14802503—
反応物3,4-Dihydro-1-naphthaleneethanamine hydrochlorideHCID 19047857—
生成物Tricyclo [3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(3,4-dihydro-1-naphthalenyl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamateHCID 86747495—

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 0.29 g (1.38 mmol) of 3,4-dihydro-1-naphthalene ethanamine hydrochloride. The purified product after chromatography was obtained as a white foam, 0.41 g (59%); 1H NMR (CDCl3) δ1.48-1.99 (17H, m), 2.39-2.50 (2H, m), 2.67-2.82 (3H, m), 3.23-3.57 (3H, m), 3.99 (2H, t, J 5.0 Hz), 4.84 (1H, br s), 5.24 (1H, br s), 5.73 (1H, m), 6.16 (1H, m), 7.00-7.63 (9H, m), 8.12 (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-5cbfd043e0054ec29ddfecea61e42edb
出典メモuspto-grants-1997_04