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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 922012생성일: 2026년 10월 25일

Morpholine → 2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide

https://huagongshe.com/reaction/922012

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물6-chloro-2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methyl-pyridine-3-carboxylic acid amideHCID 86664314—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amideHCID 5695201875%

반응 조건

온도120 °C

반응 단계

A mixture of 1.5 g (4.4 mmol) 6-chloro-2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methyl-pyridine-3-carboxylic acid amide and 1.9 ml (22.1 mmol) morpholine was heated in the microwave at 120° C. for 30 min. Subsequently the RM was diluted with water and EtOAc and the layers were separated. The organic layer was washed with a 1M aq. NaOH sol. and brine, dried over MgSO4 and concentrated in vacuo. Crystallisation (hexane/EtOAc 3:1) of the residue yielded 1.3 g (3.3 mmol, 75%) 2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide (example 2). [M+H]+ 390.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278103B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-4bc20604dcfd4863aa5fffec3c47f37a
출처 메모uspto-grants-2016_03