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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39105생성일: 2026년 10월 24일

Triethylamine → (S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester

https://huagongshe.com/ko/reaction/39105

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(Pyridin-4-yl)boronic acidHCID 2734379—
반응물Boc-Tyr-OMeHCID 7019130—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl esterHCID 6692273720.7%

반응 단계

(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionic acid methyl ester (8.46 mmol), 4-pyridyl boronic acid (29.6 mmol), Cu(OAc)2 (16.9 mmol), and molecular sieves were suspended in 25 mL of DCM. Triethylamine (59.2 mmol) was added and the mixture stirred at rt for 10 h. The mixture was diluted with ethyl acetate and washed with 10% sodium carbonate (6×). The organic layer was dried and concentrated under reduced pressure. The residue was purified over silica gel (hexanes-EtOAc) to provide (S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester (653 mg). LC-MS (m/z) 374.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524708B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-31136d61399842a4b2875e65d3f6f1cd
출처 메모uspto-grants-2013_09