関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Isopropyl chloroformate | HCID 7917 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | Pyridazine-3-carboxylic acid | HCID 269369 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Pyridazine-3-carboxamide | HCID 222902 | 20.4% |
反応手順
To a cooled solution of pyridazine-3-carboxylic acid (1.0 g, 8.06 mmol) in tetrahydrofuran (40 mL) in a dry-ice bath was added 4-methyl-morpholine (0.9 g, 8.87 mmol) and isopropyl chloroformate (1.1 g, 8.87 mmol) slowly. The reaction was stirred at −30° C. for 6 hours, then an aqueous solution of ammonia (8 mL, 10% W/W) was added. The resulting mixture was stirred at room temperature overnight, washed with a saturated aqueous solution of potassium bisulfate (50 mL). The aqueous layer was extracted with ethyl acetate (30 mL×3). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford 202.5 mg of the desired product (yield was 20.4%). MS obsd. (ESI+) [(M+H)+] 124, 1H NMR (400 MHz, CD3OD) δ ppm 9.45-9.35 (t, J=1.6 Hz, 1 H), 8.58 (s, 1 H), 8.23-8.15 (d, J=7.6 Hz, 1 H), 7.98-7.88 (m, 2 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08871756B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-2c2d9e192f20410fb389d7ec9596fc79 |
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| 出典メモ | uspto-grants-2014_10 |
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