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HRID 324740作成日:2026年10月26日

Triethylamine → Isopropyl 3-nitro-4-(3-(1-piperidinyl)anilino)benzoate

https://huagongshe.com/reaction/324740

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Isopropyl 4-chloro-3-nitrobenzoateHCID 693119—
反応物3-(Piperidin-1-yl)anilineHCID 7127806—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Isopropyl 3-nitro-4-(3-(1-piperidinyl)anilino)benzoateHCID 2274193154.1%

反応条件

温度80 °C

反応手順

To a mixture of isopropyl 4-chloro-3-nitrobenzoate (3.0 g, 12.3 mmol) and 2a (2.16 g, 12.3 mmol) in anhydrous NMP (5 ml) was added triethylamine (1.71 ml, 12.3 mmol) and the mixture was stirred at 80° C. under a stream of nitrogen overnight. The cooled mixture was partitioned between ethyl acetate and water. The organic phase was extracted with diluted hydrochloric acid (4M). The aqueous extract was rendered alkaline by addition of aqueous sodium hydroxide (12M) and extracted with ethyl acetate. This organic extract was dried over sodium sulfate and concentrated under reduced pressure. The residue was chromatographied on silica gel using a mixture of ethyl acetate and petroleum ether (1:1 v/v) as the eluent to yield isopropyl 3-nitro-4-(3-(1-piperidinyl)anilino)benzoate (2.55 g, 54%) as a red oil. This intermediate product was dissolved in ethanol (50 ml) hydrogenated at ambient pressure. The resulting diamine was treated with formic acid (25 ml) at 80° C. for 1 hour. The reaction mixture was poured into water (100 ml) and rendered alkaline by addition of aqueous sodium hydroxide (10M). The crude product was filtered off, washed with water and dried. Purification was achieved by treatment with activated carbon in refluxing 2-propanol followed by trituration with diethyl ether. Yield of 4e1: 1.27 g (53%). M.p. 160-161° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218547B1
出典データセットuspto-grants-2001_04
ORD IDord-450fdd6a93824dd3a5456d308f84366f
出典メモuspto-grants-2001_04