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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253417생성일: 2026년 10월 26일

Water → (4-Benzyloxy-2-fluoro-5-methoxy-phenyl)-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanol

https://huagongshe.com/reaction/253417

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-Benzyloxy-2-fluoro-5-methoxy-benzaldehydeHCID 561456—
반응물3-Iodo-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridineHCID 24229227—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물(4-Benzyloxy-2-fluoro-5-methoxy-phenyl)-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanolHCID 5808729597.5%

반응 조건

온도-20 °C

반응 단계

3-Iodo-1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine (68, 620 mg, 1.5 mmol, prepared as described in Example 22) was dissolved in tetrahydrofuran (15 mL) at −20° C. under an atmosphere of nitrogen. Isopropylmagnesium chloride (2.0 M in tetrahydrofuran, 840 μL) was added to the reaction. The reaction was stirred for 1.5 hours, during which the temperature rose to 5° C. The reaction was cooled to −20° C. 4-Benzyloxy-2-fluoro-5-methoxy-benzaldehyde (83, 250 mg, 0.9606 mmol) in tetrahydrofuran (5.0 mL) was added to the reaction. The reaction was stirred for 2.5 hours during which time the temperature rose to 5° C. The reaction was poured into water. The mixture was extracted with ethyl acetate. The organic layer was dried over an hydrous sodium sulfate, and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 2-25% ethyl acetate in hexane to provide compound as a white solid (84, 501 mg, 63%). MS (ESI) [M+H+]+=535.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872018B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-6d695476114d42e58f9fa197eb106b75
출처 메모uspto-grants-2011_01