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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551897생성일: 2026년 10월 25일

Tris(hydroxymethyl)aminomethane → Methyl {4-[({[(4-tert-butylphenyl)amino]carbonyl}{4-[(4-butylphenyl)-ethynyl]benzyl}amino)methyl]phenoxy}acetate

https://huagongshe.com/reaction/551897

반응식

참여 물질

역할이름HCID투입량
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물MorpholineHCID 8083—
반응물1-Tert-butyl-4-isocyanatobenzeneHCID 2735695—
반응물Methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]phenoxy}acetateHCID 57554567—
용매DichloromethaneHCID 6344—
생성물Methyl {4-[({[(4-tert-butylphenyl)amino]carbonyl}{4-[(4-butylphenyl)-ethynyl]benzyl}amino)methyl]phenoxy}acetateHCID 11541808—

반응 단계

A solution of methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]phenoxy}acetate (45 mg, 0.10 mmol) and 4-tert-butylphenylisocyanate (Aldrich, 27 mg, 0.15 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). Trisamine resin (1.2 eq, Novabiochem, 3.5 mmol/g) was then added and the mixture was stirred at rt for an additional 2 hrs. The reaction mixture was then filtrated and the solvent was removed under reduced pressure to give quantitatively the title compound. HPLC, Rt: 5.97 min purity: 96.3%). M+(ESI): 619.6, M−(ESI): 616.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947851B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-e3844b273548408292ebf116bfd0dabc
출처 메모uspto-grants-2011_05