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Ethanol → N-(4-methoxyphenyl)-N,2-dimethylpteridin-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 1,4-Dioxane-2,3-diol | HCID 96170 | — |
| 反応物 | 6-Chloro-2-methylpyrimidine-4,5-diamine | HCID 594145 | — |
| 反応物 | 4-Chloro-2-methylpteridine | HCID 22893792 | — |
| 生成物 | N-(4-methoxyphenyl)-N,2-dimethylpteridin-4-amine | HCID 46883988 | 97% |
反応手順
4-Chloro-2-methyl-pteridine. A mixture of 6-chloro-2-methyl-pyrimidine-4,5-diamine (37 mg, 0.233 mmol) and 1,4-dioxane-2,3-diol (32 mg, 0.266 mmol) in 0.8 mL of absolute ethanol was stirred at room temperature for 2 h. The reaction mixture was evaporated to dryness and the residue was purified by column chromatography (50% ethyl acetate/hexane) to give the title compound (41 mg, 0.227 mmol, 97%). 1H NMR (CDCl3): 9.24 (d, J=1.8, 1H), 9.05 (d, J=1.5, 1H), 2.99 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07618975B2 |
| 出典データセット | uspto-grants-2009_11 |
| ORD ID | ord-3a2818827ce64f1a9dba807c5a7c6b5f |
| 出典メモ | uspto-grants-2009_11 |