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Diisopropylethylamine → N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (4,4-Difluorocyclohexyl)amine | HCID 3847030 | — |
| 反応物 | 4-Chloro-8-nitroquinazoline | HCID 11458471 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amine | HCID 71678050 | 61.2% |
反応手順
A solution of 4-chloro-8-nitroquinazoline (Intermediate-7, step 2, 200 mg, 0.954 mmol), 4,4-difluorocyclohexanamine (491 mg, 2.86 mmol) and DIPEA (367 mg, 2.86 mmol) in iPrOH (2 mL) was heated in a sealed tube at 80° C. for 2 h. Then the reaction mixture was quenched with water at rt and was extracted with CHCl3. The organic layer was separated, dried, filtered and concentrated. The concentrate was purified by column chromatography using 3-5% EtOAc in CHCl3 to afford 180 mg of the title product. 1H NMR (300 MHz, DMSO d6): δ 8.59-8.55 (m, 2H), 8.43-8.40 (d, J=7.2 Hz, 1H), 8.27-8.25 (d, J=7.8 Hz, 1H), 7.69-7.63 (t, J=7.8 Hz, 1H), 4.41 (m, 1H), 2.26-2.00 (m, 6H), 1.75-1.71 (m, 2H); MS (m/z): 309.18 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09006257B2 |
| 出典データセット | uspto-grants-2015_04 |
| ORD ID | ord-0921096d044e42d59ec9c1b94892f827 |
| 出典メモ | uspto-grants-2015_04 |