関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Pentanamine | HCID 12019 | — |
| 反応物 | 4,6-Dichloro-2-methyl-5-nitropyrimidine | HCID 83192 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6-Chloro-2-methyl-5-nitro-N-(pentan-3-yl)pyrimidin-4-amine | HCID 15908584 | 35.9% |
反応手順
A mixture of 2-methyl-5-nitro-4,6-dichloro-pyrimidine (208 mg, 1.00 mmol) and 1-ethyl-propyl-amine (87 mg, 1.03 mmol) in 2 ml of dry THF was stirred at −78° C. for 4 hours. The mixture was quenched with water and extracted with ethyl acetate. The organic layer was washed with brine, dried and concentrated to give a green oil. The oil was purified through silica gel column chromatography using chloroform to 1:1 hexane/chloroform as eluent to give the title compound (93 mg, 35%). 1H NMR (CDCl3) δ 7.50 (brs, 1H), 4.29 (m, 1H), 2.51 (s, 3H), 1.4–1.8 (m, 4H), 0.92 (t, 6H) ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07125880B1 |
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| 出典データセット | uspto-grants-2006_10 |
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| ORD ID | ord-c4a27440903a4bcaaa60e26bdfc72ab8 |
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| 出典メモ | uspto-grants-2006_10 |
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