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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 398561생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-[1,2,4]triazin-3-yl-propionamide

https://huagongshe.com/reaction/398561

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물3-Amino-1,2,4-triazineHCID 70715—
반응물3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
용매PyridineHCID 1049—
생성물3-cyclopentyl-2-(3,4-dichlorophenyl)-N-[1,2,4]triazin-3-yl-propionamideHCID 223152318%

반응 조건

온도25 °C

반응 단계

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (prepared as in Example 38A, 400 mg, 1.40 mmol) in dry pyridine (5 mL) was treated with 1,3-dicyclohexylcarbodiimide (316 mg, 1.53 mmol). The reaction mixture was stirred at 25° C. for 3.5 h and then treated with 3-amino-1,2,4-triazine (296 mg, 3.08 mmol) and an additional amount of pyridine (1 mL). The reaction mixture was warmed at 100° C. for 20 h. The reaction mixture was concentrated in vacuo to remove pyridine. The resulting residue was diluted with ethyl acetate then filtered. The filtrate was washed with a 1N aqueous hydrochloric acid solution and washed with water. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 ethyl acetate/hexanes) afforded 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-[1,2,4]triazin-3-yl-propionamide (40.9 mg, 8%) as a yellow-orange solid: mp 81-83° C.; EI-HRMS m/e calcd for C17H18Cl2N4O (M+) 364.0858, found 364.0857.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610846B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-559d42a266db4746b25b9f7f0b0516e8
출처 메모uspto-grants-2003_08