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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1983554생성일: 2026년 10월 26일

Ethyl Acetate → 1-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridin-5-ol

https://huagongshe.com/reaction/1983554

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물1-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-5-methoxy-1h-pyrrolo[2,3-b]pyridineHCID 57713030—
용매DichloromethaneHCID 6344—
생성물1-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridin-5-olHCID 57713027113%

반응 단계

850 mg 1-[4-Butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethyl]-5-methoxy-1H-pyrrolo[2,3- b]pyridine was dissolved in 50 ml dichloromethane. At −78° C. 1.90 ml of a 1 molar solution of borontribromide in dichloromethane was added. The reaction mixture was allowed to warm up to room temperature. Then the reaction mixture was heated under reflux for additional two hours. 150 ml ethyl acetate were added and the mixture washed with 50 ml of a one molar solution of hydrochloric acid. The organic layer was dried over MgSO4 and the solvent removed under reduced pressure. The residue was purified by RP-HPLC to provide 930 mg 1-[4-Butyl-2-(4-trifluoromethylphenyl)-thiazol-5-ylmethyl]-1H-pyrrolo[2,3-b]pyridin-5-ol as a lyophilisate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07541464B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-9401c5c5bc7e4578a6c2c1dfde89f85f
출처 메모uspto-grants-2009_06