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O-(Diphenylphosphinyl)hydroxylamine → 2-amino-4-morpholinophthalazin-1(2H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | O-(Diphenylphosphinyl)hydroxylamine | HCID 10955453 | — |
| 反応物 | 1(2H)-Phthalazinone, 4-(4-morpholinyl)- | HCID 12689528 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-amino-4-morpholinophthalazin-1(2H)-one | HCID 70976104 | 39.5% |
反応手順
To a mixture of the product from Example 1A (0.300 g, 1.30 mmol) in THF (3.5 mL) was added a 1 M solution of potassium 2-methylpropan-2-olate in THF (1.7 mL, 1.7 mmol). The mix was stirred at room temperature for 90 minutes, and O-(diphenylphosphoryl)hydroxylamine (0.395 g, 1.70 mmol) was added and stirred overnight. The mixture was diluted with EtOAc, washed with 0.5N NaOH and water, concentrated, and chromatographed (40% EtOAc/DCM) to give 126.4 mg of product as a white solid: 1H NMR (300 MHz, DMSO-d6) δ 8.31-8.25 (m, 1H), 8.03-7.98 (m, 1H), 7.94-7.80 (m, 2H), 6.20 (s, 2H), 3.87-3.78 (m, 4H), 3.15-3.07 (m, 4H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08859549B2 |
| 出典データセット | uspto-grants-2014_10 |
| ORD ID | ord-99f319cc28084ba4a31bd398a7df37c7 |
| 出典メモ | uspto-grants-2014_10 |