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HRID 38073作成日:2026年10月26日

Ammonium Chloride → 3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine

https://huagongshe.com/reaction/38073

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1,4-Dioxane--water (1/1)HCID 21886435—
反応物6-(3-Nitro-phenyl)-7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazoleHCID 67423036—
触媒ZincHCID 23994—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamineHCID 4692918373.4%

反応条件

温度100 °C

反応手順

6-(3-Nitro-phenyl)-7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazole (150 mg, 0.463 mmol) was suspended in a 5:1 dioxane/water mixture (3 mL). Zinc powder (121 mg, 1.852 mmol, 4 eq) was added, followed by ammonium chloride (247 mg, 4.63 mmol, 10 eq) and the mixture was heated to 100° C. and stirred at the same temperature for 2 hours. The reaction mixture was then allowed to cool to room temperature and diluted with water and ethyl acetate. The aqueous phase was basified by adding solid Na2HPO4 and extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with saturated aqueous NaHCO3 and brine, dried and concentrated to dryness. 100 mg of 3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine were obtained as off-white solid (73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524707B2
出典データセットuspto-grants-2013_09
ORD IDord-466421725f78485f95cc449635479323
出典メモuspto-grants-2013_09