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Triethylamine → 3-(6-Amino-pyridine-3-carbonyl)-1-(6-bromo-pyridin-2-ylmethyl)-1H-quinolin-4-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Sodium Azide | HCID 33557 | — |
| 反応物 | Tris(2-carboxyethyl)phosphine hydrochloride | HCID 2734570 | — |
| 反応物 | HCID 57754507 | HCID 57754507 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-(6-Amino-pyridine-3-carbonyl)-1-(6-bromo-pyridin-2-ylmethyl)-1H-quinolin-4-one | HCID 57754575 | 62.7% |
反応手順
100 mg (0.22 mmol) of 1-(6-bromo-pyridin-2-ylmethyl)-3-(6-chloro-pyridine-3-carbonyl)-1H-quinolin-4-one and 72 mg (1.1 mmol) of sodium azide were heated at 100° C. in 1 mL of DMF for 1 h. The temperature of the solution was lowered to 70° C. and 1 mL of water was added, followed by 214 uL (155 mg, 1.54 mmol) of triethylamine and 378 mg (1.32 mmol) of tris(2-carboxyethyl)phosphine hydrochloride. After 1 h of reaction time the mixture was purified on reverse-phase HPLC, followed by flash chromatography to give 60 mg of a yellow powder. LC-MSD, m/z for C21H15BrN4O2 [M+H]+=435.0, 437.0; HPLC retention time: 0.6 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07557213B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-dc87f762a0db4bc2bd90e8387eb501ca |
| 出典メモ | uspto-grants-2009_07 |