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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76205생성일: 2026년 10월 25일

Potassium Carbonate → (S)-N-(1-(4-((1-Methyl-1H-pyrazol-4-yl) ethynyl)phenyl]ethyl}cyclopropane-carboxamide

https://huagongshe.com/reaction/76205

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sec-ButylamineHCID 24874—
반응물1-Methyl-1H-pyrazole-4-carbaldehydeHCID 573117—
반응물N-[1-(4-iodophenyl)ethyl]cyclopropanecarboxamideHCID 66611166—
반응물Dimethyldiazo-2-oxopropylphosphonatHCID 131731873—
촉매HCID 178418476HCID 178418476—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(S)-N-(1-(4-((1-Methyl-1H-pyrazol-4-yl) ethynyl)phenyl]ethyl}cyclopropane-carboxamideHCID 66611617—

반응 단계

To 100 mg (0.91 mmol) 1-methyl-1H-pyrazole-4-carbaldehyde in 1.00 mL MeOH are added 289 mg (2.09 mmol) K2CO3 and finally dropwise 349 mg (1.82 mmol) dimethyldiazo-2-oxopropylphosphonat (in 2.0 mL MeOH).The reaction mixture is stirred at r.t. over night. The reaction is quenched by the addition of water and EtOAc. The organic layer is separated, dried with Na2SO4 and the solvent is removed in vacuo. To the residue is added 286 mg (0.91 mmol) cyclopropanecarboxylic acid [1-(4-iodo-phenyl)-ethyl]amide (I52.2), 63.7 mg (0.09 mmol) bis-(triphenylphosphin)-palladiumdichlorid, 2.00 mL 2-butylamine and 2.00 mL water. The reaction mixture is stirred at r.t. over night. The mixture is diluted with water and extracted with DCM. The organic layer is dried with Na2SO4 and the solvent is evaporated in vacuo. The residue is purified consecutively by column chromatography (silica gel, DCM/MeOH 98:2) and HPLC (MeOH/H2O/NH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835472B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-85efdbcbf919466babcf2722626b5c22
출처 메모uspto-grants-2014_09