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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2298023생성일: 2026년 10월 24일

Guanidine Hydrochloride → HCID 178429413, 화합물

https://huagongshe.com/ko/reaction/2298023

반응식

참여 물질

역할이름HCID투입량
반응물Guanidine HydrochlorideHCID 5742—
반응물Thionyl ChlorideHCID 24386—
반응물1-(3-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 4423672—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물HCID 178429413HCID 17842941312.7%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06492401B1
출처 데이터셋uspto-grants-2002_12
ORD IDord-a3ff8d1a6c854a779f86a0b2b6980ea5
출처 메모uspto-grants-2002_12