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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1983556생성일: 2026년 10월 26일

Allyl bromide → 5-Allyloxy-1-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1983556

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Ethyl AcetateHCID 8857—
반응물Cesium carbonateHCID 10796—
반응물1-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridin-5-olHCID 57713027—
용매DimethylformamideHCID 6228—
생성물5-Allyloxy-1-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridineHCID 57713032—

반응 단계

730 mg 1-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridin-5-ol were dissolved in 20 ml dimethylformamide and 1.1 mg cesium carbonate and 410 mg allylbromide were added. The reaction mixture was stirred at room temperature for one hour then 100 ml ethyl acetate were added and the mixture was washed five times with portions of 20 ml of water The organic layer was dried over MgSO4 and the solvent removed under reduced pressure. This gives 800 mg 5-Allyloxy-1-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridine as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07541464B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-54927c94ecfd4e2981de3ebb5ba68007
출처 메모uspto-grants-2009_06