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HRID 970758作成日:2026年10月25日

2,4,6-Trifluorobenzoyl chloride → N-(6-(4-Dimethylamino-cyclohex-1-enyl)-pyridin-2-yl)-2,4,6-trifluoro-benzamide dihydrochloride salt

https://huagongshe.com/reaction/970758

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-Trifluorobenzoyl chlorideHCID 144895—
反応物6-(4-Dimethylamino-cyclohex-1-enyl)-pyridin-2-ylamineHCID 58852365—
生成物N-(6-(4-Dimethylamino-cyclohex-1-enyl)-pyridin-2-yl)-2,4,6-trifluoro-benzamide dihydrochloride saltHCID 6935106746%

反応手順

Using a method similar to example 1, using 2,4,6-trifluoro-benzoyl chloride (134 mg, 0.69 mmol) and 6-(4-dimethylamino-cyclohex-1-enyl)-pyridin-2-ylamine, isomer 2 (preparation 11, 100 mg, 0.46 mmol) provides the free amine of the title compound as an oil (80 mg, 46%): MS (ES): m/z=376.2 (M+H)+; 1H NMR (CD3OD): δ 8.25 (t, 1H), 7.67 (d, 1H), 7.74 (d, 1H), 7.12 (t, 2H), 6.81 (m, 1H), 3.62 (m, 1H), 2.96 (s, 6H), 2.73 (m, 4H), 2.45 (m, 1H), 1.95 (m, 1H). Using a salt formation method similar to that in example 1 gives the dihydrochloride salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312236B2
出典データセットuspto-grants-2007_12
ORD IDord-6d48c821c7664d75a4e53c3a1dc82ebc
出典メモuspto-grants-2007_12