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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551901생성일: 2026년 10월 25일

Tris(hydroxymethyl)aminomethane → methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}{[(E)-2-phenylvinyl]-sulfonyl}amino)methyl]phenoxy}acetate

https://huagongshe.com/reaction/551901

반응식

참여 물질

역할이름HCID투입량
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물MorpholineHCID 8083—
반응물Ethenesulfonyl chloride, 2-phenyl-HCID 107500—
반응물Methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]phenoxy}acetateHCID 57554567—
용매DichloromethaneHCID 6344—
생성물methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}{[(E)-2-phenylvinyl]-sulfonyl}amino)methyl]phenoxy}acetateHCID 1172139695%

반응 단계

A solution of methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]phenoxy}-acetate (42 mg, 0.10 mmol) and β-styrene sulfonyl chloride (Aldrich, 23 mg, 0.11 mmol) in DCM (2 mL) was stirred at rt overnight in presence of a morpholine resin (1.5 eq., Novabiochem HL, 3.8 mmol/g) (1.5 eq). Trisamine resin (1 eq, Novabiochem, 3.5 mmol/g) was then added and the mixture stirred at rt for an additional 2 hrs. The reaction mixture was then filtrated and the solvent was removed under reduced pressure to give 55 mg (95%) of the title compound. HPLC, Rt: 5.8 min (purity: 83%). M+(ESI): 608.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947851B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-8123a76cd55a4afc8455bec3c379a2f4
출처 메모uspto-grants-2011_05