戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 63593作成日:2026年10月25日

Diisopropylethylamine → 2-Amino-5-chloro-4-(4-(5-methyl-1,2,4-oxadiazol-3-yl)methylpiperazin-1-yl)-3-nitropyridine

https://huagongshe.com/reaction/63593

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2-Amino-4,5-dichloro-3-nitropyridineHCID 46867660—
反応物1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperazine hydrochlorideHCID 75530688—
溶媒IsopropanolHCID 3776—
生成物2-Amino-5-chloro-4-(4-(5-methyl-1,2,4-oxadiazol-3-yl)methylpiperazin-1-yl)-3-nitropyridineHCID 7148147370.2%

反応条件

温度45 °C

反応手順

1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperazine hydrochloride (217 mg, 0.99 mmol) and 2-amino-4,5-dichloro-3-nitropyridine (208 mg, 1.0 mmol) were stirred in 2-propanol (5 mL) and diisopropylethylamine (523 μL, 387 mg, 3.0 mmol) was added. The mixture was stirred and heated at 45° C. for 23 h. The reaction was cooled and the product filtered off and washed with 2-propanol. Drying in vacuum gave the product (246 mg, 69%). 1H-NMR (500 MHz, CDCl3), 2.63 (s, 3H, CH3), 2.77 (br m, 4H, piperazine C—H), 3.29 (m, 4H, piperazine C—H), 3.76 (s, 2H, CH2), 5.27 (s, 2H, NH2), 8.02 (s, 1H, pyridine 6-H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447092B2
出典データセットuspto-grants-2016_09
ORD IDord-ca11d6524ce540f6b793af1492dd8c08
出典メモuspto-grants-2016_09