化工社化工社 化学情報印刷レポート · 研究参考用
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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophan | HCID 14802503 | — |
| 反応物 | 3,4-Dihydro-1-naphthaleneethanamine hydrochloride | HCID 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]carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05622983 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-5cbfd043e0054ec29ddfecea61e42edb |
| 出典メモ | uspto-grants-1997_04 |