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HRID 383565作成日:2026年10月26日

Sulfuric Acid → 1-(2,4-Difluorophenyl)-1H-pyrazol-5-amine

https://huagongshe.com/reaction/383565

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物TriethylamineHCID 8471—
反応物2-ChloroacrylonitrileHCID 70198—
反応物2,4-Difluorophenylhydrazine hydrochlorideHCID 2733301—
反応物Edta disodiumHCID 44120005—
溶媒MethanolHCID 887—
生成物1-(2,4-Difluorophenyl)-1H-pyrazol-5-amineHCID 43316768—

反応条件

温度70 °C

反応手順

A 250 mL RBF containing a solution of 1-(2,4-difluorophenyl)hydrazine hydrochloride (10.33 g, 57 mmol), Et3N (8.0 mL, 57 mmol), EDTA disodium salt dihydrate (50 mg, 0.13 mmol) in 100 mL of MeOH was fitted with a reflux condenser, and heated to 70° C. To the refluxing solution was added 2-chloroacrylonitrile (5.0 mL, 57 mmol) slowly. The solution was heated at reflux for an additional 7.5 h. It was cooled to RT then concentrate sulfuric acid (5.2 mL, 97 mmol) was added slowly and the reaction mixture again heated to reflux for 18 h. The reaction mixture was cooled to 0° C. and treated with Na2CO3 monohydrate (21.00 g) and stirred at RT for 8 h. The reaction mixture was concentrated on the rotovap to remove the MeOH. The resulting rust colored solid was then treated with 100 mL of water and extracted with EtOAc (2×100 mL). The combined EtOAc layers were washed with brine, dried and concentrated. Purification of the crude material on an ISCO 120 g column (20-80% EtOAc in hexanes) afforded 1-(2,4-difluorophenyl)-1H-pyrazol-5-amine as an orange-brown viscous oil. MS (ES+): 196.1 (M+H)+. A further general description of this procedure can be found in U.S. Pat. No. 4,803,215.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367671B2
出典データセットuspto-grants-2013_02
ORD IDord-827d822dab2c4eb19f00a53b1c9daf2f
出典メモuspto-grants-2013_02