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Diisopropylethylamine → 2-[(2-Aminocyclopentyl)methylamino]-4-methoxyquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Cyclopentanemethanamine, 2-amino- | HCID 89512 | — |
| 反応物 | 2-Chloro-4-methoxyquinoline | HCID 12369166 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Ammonia | HCID 222 | — |
| 生成物 | 2-[(2-Aminocyclopentyl)methylamino]-4-methoxyquinoline | HCID 18353754 | 16% |
反応手順
(2-Aminocyclopentyl)methylamine (0.50 g, 0.00438 mol), 2-chloro-4-methoxyquinoline (0.85 g, 0.00438 mol) and N,N′-diisopropylethylamine (1 ml) were stirred together at 80° C. in a sealed tube for 16 h. After cooling the mixture was diluted in methanol then concentrated onto silica gel and purified by silica gel chromatography (5%, 10% then 20% (10% 880 aqueous ammonia in methanol) in dichloromethane) to give the title compound as a white gum (50:50 mixture of cis and trans isomers; 0.095 g, 8%). δH (CD3OD) 1.40-2.25 (7H, m, (CH2)3, CHCH2NH), 2.96-3.76 (3H, m, CHNH2, CH2NH), 4.02 (3H, s, OCH3), 6.02-6.23 (1H, 2s, 3-H), 7.13-7.95 (4H, m, ArH). MS (ES+) 272 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06320051B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-c9f95cfaedb74bd2812cae285ba83df0 |
| 出典メモ | uspto-grants-2001_11 |