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HRID 1525782作成日:2026年10月27日

Water → 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1525782

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium PermanganateHCID 23673458—
反応物HCID 118232987HCID 118232987—
溶媒tert-ButanolHCID 6386—
生成物3-chloro-1-(pyridin-3-yl)-1H-pyrazole-4-carboxylic acidHCID 8670582546%

反応条件

温度80 °C

反応手順

To a mixture of 3-(3-chloro-4-methyl-4,5-dihydro-1H-pyrazol-1-yl)pyridine (2.0 g, 10 mmol) in water (10.0 mL) and tert-butanol (5.0 mL) was added a solution of sodium permanganate (NaMnO4) (5.0 g, 35 mmol) in water (15 mL) over 20 minutes. The mixture was heated to 80° C. and stirred overnight. Additional sodium permanganate (0.711 g, 5.0 mmol) in water (2.0 mL) was added after 16 hours and the mixture was stirred for another 4 hours. The dark mixture was filtered through Celite®, washed with water (5.0 mL) and ethyl acetate (3×15 mL). The aqueous layer was extracted with ethyl acetate (25 mL) and acidified with concentrated hydrochloric acid to pH 5 leading to white precipitate which was collected by filtration. The filtrate was concentrated leading to white precipitate which was collected by filtration and washed with water (2.0 mL). The solid products were combined and dried under high vacuum to afford the title compound as a white solid (1.0 g, 46%): 1H NMR (400 MHz, DMSO-d6) δ 9.11 (s, 2H), 8.59 (d, J=4.7, 1H), 8.28 (ddd, J=8.4, 2.7, 1.4 Hz, 1H), 7.58 (dd, J=8.0, 4.4 Hz, 1H); 13C NMR (101 MHz, DMSO-d6) δ 162.24, 148.35, 141.46, 140.21, 135.01, 134.01, 126.45, 124.23, 115.34; ESIMS m/z 224 ([M+H]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09085552B1
出典データセットuspto-grants-2015_07
ORD IDord-b0935a88b5dc47b9a2adf3ce09cc5165
出典メモuspto-grants-2015_07