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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469089생성일: 2026년 10월 25일

Methanol → 4-Methoxy-N,2,6-trimethyl-N-[(5-{[4-(3-pyrrolidin-1-ylpropyl)piperazin-1-yl]carbonyl}-1,3,4-oxadiazol-2-yl)methyl]benzenesulfonamide

https://huagongshe.com/reaction/469089

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물1-(3-Pyrrolidinopropyl)PiperazineHCID 2737252—
반응물TrimethylaluminumHCID 16682925—
반응물Methyl 5-({[(4-methoxy-2,6-dimethylphenyl)sulfonyl](methyl)amino}methyl)-1,3,4-oxadiazole-2-carboxylateHCID 67217606—
용매TetrahydrofuranHCID 8028—
생성물4-Methoxy-N,2,6-trimethyl-N-[(5-{[4-(3-pyrrolidin-1-ylpropyl)piperazin-1-yl]carbonyl}-1,3,4-oxadiazol-2-yl)methyl]benzenesulfonamideHCID 58393208—

반응 조건

온도-40 °C

반응 단계

1-(3-Pyrrolidin-1-ylpropyl)piperazine (128 mg, 1.65 mmol) was dissolved in THF (5 mL) and the resulting solution was cooled to −40° C. prior to the addition of trimethylaluminium (2 M in toluene, 0.59 mL). The reaction was stirred for 15 min at −40° C. and a solution of methyl 5-({[(4-methoxy-2,6-dimethylphenyl)sulfonyl](methyl)amino}methyl)-1,3,4-oxadiazole-2-carboxylate (200 mg, 0.54 mmol) in THF (5 mL) was added dropwise. The reaction was stirred at ambient temperature for 18 h and MeOH (5 mL) was added. The solvents were removed in vacuo and the resulting residue was purified by FCC, eluting with 0-2% MeOH in DCM to afford the title compound as a pale yellow semi solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623859B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-2281eb1867284a5ca0e93fe9947c5ae1
출처 메모uspto-grants-2014_01