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HRID 872537作成日:2026年10月26日

Hydrochloric Acid → 3-tert-butyl-N-(2-(5-(3-chloro-4-cyano-2-methylphenyl)furan-2-yl)ethyl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/872537

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-Amino-2-chloro-3-methylbenzonitrileHCID 21875413—
反応物Sodium NitriteHCID 23668193—
反応物3-tert-butyl-N-(2-(furan-2-yl)-ethyl)-1H-pyrazole-5-carboxamideHCID 178441080—
触媒Ferrous chloride tetrahydrateHCID 16211588—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物3-tert-butyl-N-(2-(5-(3-chloro-4-cyano-2-methylphenyl)furan-2-yl)ethyl)-1H-pyrazole-5-carboxamideHCID 1784219592.6%

反応条件

温度80 °C

反応手順

4-amino-2-chloro-3-methylbenzonitrile (0.200 g, 1.20 mmol) was added to a solution of water (2 ml) and conc. HCl (2 ml) and the mixture was stirred vigorously, heated to 80° C. for 15 min and then cooled to −10° C. Sodium nitrite (0.091 g, 1.32 mmol) was dissolved in 0.5 ml of water and added drop wise to the cooled reaction mixture. After 40 min, the mixture was filtered and 3-tert-butyl-N-(2-(furan-2-yl)-ethyl)-1H-pyrazole-5-carboxamide (0.345 g, 1.32 mmol) dissolved in acetone (3 ml) was added to the filtrate. Then, a solution of iron (II) chloride tetrahydrate in water (3 ml) was added portion wise and the mixture was stirred for 15 h at RT. Water (25 ml) was added to the reaction mixture and extracted three times with EtOAc. The combined organic layers were washed with saturated aqueous NaHCO3 and water and dried with Na2SO4, filtered and evaporated to dryness. CombiFlash purification afforded 0.013 g of the title compound. 1H-NMR (400 MHz; d6-DMSO): δ 1.34 (s, 9H), 3.03 (t, 2H), 3.77 (m, 2H), 6.28 (d, 1H), 6.62 (m, 2H), 7.12 (m, 1H), 7.50 (d, 1H), 7.65 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08975254B2
出典データセットuspto-grants-2015_03
ORD IDord-69754be82c7c477e94d23066f3fe62a7
出典メモuspto-grants-2015_03