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HRID 80910作成日:2026年10月24日

2-Chloropropane → 1-Isopropyl-4-[6-(4-trifluoromethylphenyl)pyridazin-3-yl]-[1,4]diazepane, dihydrochloride

https://huagongshe.com/ja/reaction/80910

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChloropropaneHCID 6361—
反応物TriethylamineHCID 8471—
反応物Sodium hydrideHCID 24758—
反応物4-[6-(4-Trifluoromethylphenyl)pyridazin-3-yl][1,4]diazepane, dihydrochlorideHCID 131730778—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物1-Isopropyl-4-[6-(4-trifluoromethylphenyl)pyridazin-3-yl]-[1,4]diazepane, dihydrochlorideHCID 13173077721%

反応手順

4-[6-(4-Trifluoromethylphenyl)pyridazin-3-yl][1,4]diazepane, dihydrochloride (0.028 g, 0.071 mmol) was suspended in THF (4 mL) and triethylamine (0.022 g, 0.21 mmol) was added. Sodium hydride (0.0085 g, 0.35 mmol) was added and the reaction mixture was stirred at rt for 20 min. Dry N,N-dimethylformamide (1 mL) and 2-chloropropane (0.056 g, 0.71 mmol) was added and the reaction mixture was heated 30 min at 160° C. and 30 min at 180° C. in a microwave oven. The reaction mixture was purified on a silicagel column (0.04-0.063 mesh) using dichloromethane/MeOH (9:1) as eluent. This afforded a crude oil containing several components that was purified further by preparative HPLC using Method B. This afforded 9 mg of an oil which was dissolved into MeOH. Addition of HCl in diethyl ether afforded 6.5 mg (21%) of the title compound as an oily dihydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846677B2
出典データセットuspto-grants-2014_09
ORD IDord-48faf4b9d2b044d9ba597e68eb6d8c3d
出典メモuspto-grants-2014_09