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HRID 22937作成日:2026年10月24日

Tetrahydrofuran → HCID 178511612、化合物

https://huagongshe.com/ja/reaction/22937

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物2-Chloro-5-nitropyridineHCID 78308—
反応物HCID 178511674HCID 178511674—
溶媒EthanolHCID 702—
生成物HCID 178511612HCID 178511612—

反応手順

A solution of 5-nitro-2-chloropyridine (2.50 g) and trans-1,4-cyclohexanediamine (5.40 g) in ethanol (15 ml)-tetrahydrofuran (10 ml) was stirred at room temperature for 5 days. The precipitates were removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (solvent: chloroform-methanol-concentrated aqueous ammonia (20:4:1)) and crystallized from ethyl acetate to obtain N-(5-nitro-2-pyridyl)-trans-1,4-cyclohexanediamine (Reference Example 3-1 in Table 5).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849622B2
出典データセットuspto-grants-2005_02
ORD IDord-c736fbffea7a41fb8eec7294aa7c060f
出典メモuspto-grants-2005_02