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HRID 1245763作成日:2026年10月26日

3-Pentanamine → 6-Chloro-2-methyl-5-nitro-N-(pentan-3-yl)pyrimidin-4-amine

https://huagongshe.com/reaction/1245763

反応式

関与物質

役割名称HCID仕込み量
反応物3-PentanamineHCID 12019—
反応物4,6-Dichloro-2-methyl-5-nitropyrimidineHCID 83192—
溶媒TetrahydrofuranHCID 8028—
生成物6-Chloro-2-methyl-5-nitro-N-(pentan-3-yl)pyrimidin-4-amineHCID 1590858435.9%

反応条件

温度-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07125880B1
出典データセットuspto-grants-2006_10
ORD IDord-c4a27440903a4bcaaa60e26bdfc72ab8
出典メモuspto-grants-2006_10