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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25946생성일: 2026년 10월 23일

Pyruvic Acid → 2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone

https://huagongshe.com/ko/reaction/25946

반응식

참여 물질

역할이름HCID투입량
반응물Pyruvic AcidHCID 1060—
반응물Thionyl ChlorideHCID 24386—
반응물Sodium BicarbonateHCID 516892—
반응물2',5-dichloro-3-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromideHCID 21325684—
용매BenzeneHCID 241—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenoneHCID 2132574464.8%

반응 단계

A solution of pyruvic acid (0.33 g) and thionyl chloride (0.27 g) in chloroform (2 ml) is refluxed for 1 hour. After cooling, the solution is mixed with 2',5-dichloro-3-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromide (1.31 g), benzene (6 ml) and dimethylformamide (11 ml) at 0° C. The resultant mixture is stirred at room temperature for 3 hours and allowed to stand overnight. The reaction mixture is neutralized with aqueous sodium bicarbonate and shaken with ethyl acetate. The organic layer is washed with water, dried and evaporated to remove the solvent. The residue is recrystallized from ethyl acetate to give 2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone (0.7 g) as crystals melting at 178° to 180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147700
출처 데이터셋uspto-grants-1979_04
ORD IDord-9ffa1233d3a54301a7b399e8045faf43
출처 메모uspto-grants-1979_04