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HRID 1676533作成日:2026年10月26日

Diisopropylethylamine → 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide

https://huagongshe.com/reaction/1676533

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物3-Isopropoxy-4-nitrobenzoic acidHCID 602928—
反応物4-Amino-1-methylpiperidineHCID 2737531—
反応物HCID 178484289HCID 178484289—
溶媒DimethylformamideHCID 6228—
溶媒Sodium CarbonateHCID 10340—
生成物3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamideHCID 6707640195.7%

反応手順

To a mixture of 0.88 g (3.9 mmole) of 3-isopropoxy-4-nitro-benzoic acid, 2.8 mL (16 mmole) of ethyldiisopropyl amine, 0.54 g (4.7 mmole) of 4-amino-1-methyl-piperidine and 18 mL of dimethylformamide was added 1.63 g (4.3 mmole) of 1-[bis(dimethylamino)methylene)-1H-benzotriazolium 3-oxide hexafluorophosphate. The mixture was stirred at room temperature for 2 hours, then diluted with ice water and saturated sodium carbonate. The mixture was extracted with ethyl acetate 3 times. The combined organic layers were washed three times with sodium carbonate, three times with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 100:0-40:60) gave 1.2 g of 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08003785B2
出典データセットuspto-grants-2011_08
ORD IDord-9a8a08cb7178483b9f4aea6a46c0219a
出典メモuspto-grants-2011_08