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1-(2-(Dimethylamino)ethyl)-5-oxopyrrolidine-3-carboxylic acid → 1-(2-dimethylamino-ethyl)-5-oxo-pyrrolidine-3-carboxylic acid (6-chloro-7-methoxy-9H-beta-carbolin-8-yl)-amide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(2-(Dimethylamino)ethyl)-5-oxopyrrolidine-3-carboxylic acid | HCID 654521 | — |
| 反応物 | 6-Chloro-7-methoxy-9h-pyrido[3,4-b]indol-8-amine | HCID 21362743 | — |
| 生成物 | 1-(2-dimethylamino-ethyl)-5-oxo-pyrrolidine-3-carboxylic acid (6-chloro-7-methoxy-9H-beta-carbolin-8-yl)-amide | HCID 11270353 | 60% |
反応手順
Prepared according to Method A from 6-chloro-7-methoxy-9H-β-carboline-8-ylamine and 1-(2-dimethylamino-ethyl)-5-oxo-pyrrolidine-3-carboxylic acid in 60% yield following purification using a semi-preparative Chiralcel OD column with 85/7.5/7.5 hexane/EtOH/MeOH as the eluant. 1H-NMR (300 MHz, DMSO-d6): δ 2.44 (s, 6H), 2.75 (t, 2H), 2.88 (d, 2H), 3.56 (t, 2H), 3.66 (m, 1H), 3.85 (m, 2H), 3.90 (s, 3H), 8.03 (d, 1H), 8.21 (s, 1H), 8.28 (d,1H), 8.79 (s,1H). Retention Time (LC, method: ammonium acetate standard): 1.42 min. MS (M+H+): 430.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07951801B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-1885f67f08e044f499f82fa9fd7195b7 |
| 出典メモ | uspto-grants-2011_05 |