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2-Amino-4-chloro-6-methylpyrimidine → 2-Amino-4-[(4-{[(4-amino-2-methyl-6-quinolinyl)carbonyl]amino}benzyl)amino]-6-methylpyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-4-chloro-6-methylpyrimidine | HCID 21810 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4-{[(4-Amino-2-methyl-6-quinolinyl)carbonyl]amino}benzylamine | HCID 17864630 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-Amino-4-[(4-{[(4-amino-2-methyl-6-quinolinyl)carbonyl]amino}benzyl)amino]-6-methylpyrimidine | HCID 10341661 | 82.2% |
反応手順
The solution of 27 mg (0.05 mmol) 4-{[(4-amino-2-methyl-6-quinolinyl)carbonyl]amino}benzylamine, 15 mg (0.1 mmol) 2-amino-4-chloro-6-methylpyrimidine, and 0.05 ml (0.3 mmol) diisopropyl ethylamine in 1 ml DMF was stirred at 120° C. for 5 h. After evaporation of the solvent the residue was purified by HPLC and lyophilized to yield 17 mg (51%) of the title compound. MS 414.3 (M+1)+, 1H-NMR (DMSO-d6) δ 2.19 (s, 3H), 2.60 (s, 3H), 4.56 (d, 2H), 5.94 (s, 1H), 6.65 (s, 1H), 7.33 (d, 2H), 7.75 (d, 2H), 7.88 (d, 1H), 8.35 (d, 1H), 8.97 (s, 1H), 8.96–9.01 (m, 2H), 10.51 (s, 1H), 12.30 (br. 1H), 13.60(br. 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07235558B2 |
| 出典データセット | uspto-grants-2007_06 |
| ORD ID | ord-dc18de0a4ae04d8393cbfd263c242ddc |
| 出典メモ | uspto-grants-2007_06 |