돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1469369생성일: 2026년 10월 26일

Boron tribromide → 3-{5-[3-(2-Hydroxy-ethoxy)-phenyl]-pyridin-2-yloxy}-azetidine-1-carboxylic acid pyridazin-3-ylamide

https://huagongshe.com/reaction/1469369

반응식

참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물3-{5-[3-(2-Benzyloxy-ethoxy)-phenyl]pyridin-2-yloxy}-azetidine-1-carboxylic acid pyridazin-3-ylamideHCID 44218899—
용매DichloromethaneHCID 6344—
생성물3-{5-[3-(2-Hydroxy-ethoxy)-phenyl]-pyridin-2-yloxy}-azetidine-1-carboxylic acid pyridazin-3-ylamideHCID 442188985%

반응 조건

온도0 °C

반응 단계

3-{5-[3-(2-Benzyloxy-ethoxy)-phenyl]-pyridin-2-yloxy}-azetidine-1-carboxylic acid pyridazin-3-ylamide (Example 9, 325 mg, 0.65 mmol) was dissolved in anhydrous dichloromethane (10 mL) under a nitrogen atmosphere. The mixture was cooled with an ice water bath and boron tribromide in dichloromethane solution (1M, 0.98 mL, 0.98 mmol) was added drop-wise affording a precipitate. The reaction mixture was stirred at 0° C. for 2 hr. The precipitate was collected by filtration and purified by flash chromatography on silica gel eluting with ethyl acetate, then 5-10% methanol in DCM. Further purification by preparative HPLC at pH4 afforded title compound (13 mg, 5%) as colourless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006269B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-9ec04271437449cebb90402fd984c786
출처 메모uspto-grants-2015_04