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HRID 2298023作成日:2026年10月26日

Guanidine Hydrochloride → HCID 178429413、化合物

https://huagongshe.com/reaction/2298023

反応式

関与物質

役割名称HCID仕込み量
反応物Guanidine HydrochlorideHCID 5742—
反応物Thionyl ChlorideHCID 24386—
反応物1-(3-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 4423672—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物HCID 178429413HCID 17842941312.7%

反応手順

A mixture of 5-methyl-1-(3-chlorophenyl)pyrazole-4-carboxylic acid (234 mg, 1.0 mmol) and 5 ml SOCl2 was heated to reflux for 45 min. Excess SOCl2 was removed in vacuo via codistillation with toluene. The residue was dissolved in 2mL of anhydrous THF and added dropwise over 30 minutes to a vigorously stirred 40° C. solution of guanidine hydrochloride (344 mg, 3.6 mol) in 3.25 mL 2 N NaOH and 1.9 mL THF. The resulting mixture was heated to reflux for 4 hours and then cooled. The organic solvent was removed in vacuo. The residue was diluted with 10 mL 1 N NaOH and extracted with 5×5 mL EtOAc. The combined organic layers were dried (Na2SO4) filtered and concentrated in vacuo to a white solid. This material was dissolved in 1 mL MeOH and 18.4 μL 12 N HCl was added with stirring. The solvents were removed in vacuo with toluene azeotropes and the resulting solid was stirred in 1 mL ether/acetone (1:1) and filtered to remove residual H2O. Drying under high vacuum at 40° C. afforded the desired product (20 mg, 6%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06492401B1
出典データセットuspto-grants-2002_12
ORD IDord-a3ff8d1a6c854a779f86a0b2b6980ea5
出典メモuspto-grants-2002_12