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HRID 30221作成日:2026年10月25日

Acetic Acid → 2,4,6-Trifluoro-N-[6-(1-propylpiperidin-4-ylcarbonyl)-pyridin-2-yl]-benzamide

https://huagongshe.com/reaction/30221

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PropanalHCID 527—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2,4,6-trifluoro-N-(6-(piperidine-4-carbonyl)pyridin-2-yl)benzamideHCID 17980337—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物2,4,6-Trifluoro-N-[6-(1-propylpiperidin-4-ylcarbonyl)-pyridin-2-yl]-benzamideHCID 17980372—

反応手順

Mix 2,4,6-trifluoro-N-[6-(piperidin-4-ylcarbonyl)-pyridin-2-yl]-benzamide (50 mg), propionaldehyde (80 mg), sodium triacetoxyborohydride (38 mg) and acetic acid (21 mg) with dichloromethane (5 mL) and stir for 1.5 hrs. Dilute with methanol and load on a SCX column (10 g), wash with methanol, elute the product with 2M NH3-methanol. Purify the product on a silica gel column (10 g, dichloromethane/2M NH3 in methanol, gradient) to obtain the title compound as a free base (26 mg). Mass spectrum (electrospray) m/z=406 (M+1); 1H NMR (CDCl3): 8.52 (d, 1H), 8.38 (br, 1H), 7.92 (t, 1H), 7.82 (dd, 1H), 6.82 (m, 2H), 3.61 (br, 1H), 3.00 (m, 2H), 2.34 (m, 2H), 2.11 (m, 2H), 1.87 (m, 3H), 1.60 (m, 5H), 0.90 (t, J=7.3 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423050B2
出典データセットuspto-grants-2008_09
ORD IDord-53028720ace14c31b69b2f543274351c
出典メモuspto-grants-2008_09