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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43393생성일: 2026년 10월 24일

1,2-Dichloroethane → 4-[5-({(3S)-4-[(4-Chlorophenyl)sulfonyl]-3-methyl-1-piperazinyl}carbonyl)-2-pyridinyl]morpholine

https://huagongshe.com/ko/reaction/43393

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물EthylmorpholineHCID 7525—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물6-Morpholinonicotinic AcidHCID 2776460—
반응물(2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methylpiperazine hydrochlorideHCID 67028562—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-[5-({(3S)-4-[(4-Chlorophenyl)sulfonyl]-3-methyl-1-piperazinyl}carbonyl)-2-pyridinyl]morpholineHCID 5916136756%

반응 단계

To a suspension of (2S)-1-[(4-chlorophenyl)sulfonyl]-2-methylpiperazine hydrochloride (Description 4) (105 mg, 0.338 mmol), EDC (71.3 mg, 0.372 mmol), HOBT.H2O (56.9 mg, 0.372 mmol) and 6-(4-morpholinyl)-3-pyridinecarboxylic acid (77 mg, 0.372 mmol) in DCM (5 ml) was added N-ethyl morpholine (0.090 mL, 0.710 mmol). The reaction was stirred for 18 h at ambient temperature. To the reaction was added water (3 ml) and the organic layer collected via a hydrophobic frit. The organic layer was reduced in volume to approximately 2 ml then loaded onto a silica SP4 chromatography cartridge. The cartridge was eluted with a gradient from 60% ethyl acetate in iso-hexane to ethyl acetate then ethyl acetate. Fractions containing the desired product were combined and reduced in vacuo to yield the title compound as a white solid (88 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536183B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-7fd85d7d94ec4a5893781fa041069bcc
출처 메모uspto-grants-2013_09