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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430196생성일: 2026년 10월 27일

Diisopropylethylamine → 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-pyridazin-3-yl-propionamide

https://huagongshe.com/reaction/430196

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물AminopyridazineHCID 230373—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
용매DimethylformamideHCID 6228—
생성물3-cyclopentyl-2-(3,4-dichlorophenyl)-N-pyridazin-3-yl-propionamideHCID 992899762.2%

반응 단계

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (prepared in Example 38, 625.2 mg, 2.18 mmol), O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (908.3 mg, 2.39 mmol), N,N-diisopropylethylamine (1.1 mL, 6.53 mmol), and 3-aminopyridazine (310.6 mg, 3.27 mmol) in dry N,N-dimethylformamide (11 mL) was stirred at 25° C. under nitrogen for 72 h. The reaction mixture was concentrated in vacuo to remove N,N-dimethylformamide. The resulting residue was diluted with ethyl acetate (200 mL). The organic layer was washed with a 10% aqueous hydrochloric acid solution and washed with a saturated aqueous sodium chloride solution. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-pyridazin-3-yl-propionamide (493.8 mg, 62%) as a white foam: mp 70-71° C.; EI-HRMS m/e calcd for C18H19Cl2N3O (M+) 363.0905, found 363.0908.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06320050B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-580c8d0f801a42bc85bdf4585076a378
출처 메모uspto-grants-2001_11