돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445926생성일: 2026년 10월 24일

Phosphorus oxychloride → (4-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)methanol

https://huagongshe.com/ko/reaction/1445926

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물Ethyl 4-methoxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylateHCID 11736140—
반응물1-benzyl-2-methyl-1H-pyrroleHCID 12643084—
반응물1-benzyl-5-methyl-1H-pyrrole-2-carbaldehydeHCID 59170380—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물(4-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)methanolHCID 15885418—
생성물1-benzyl-5-methyl-1H-pyrrole-2-carbaldehydeHCID 59170380—

반응 단계

1-Benzyl-5-methyl-1H-pyrrole-2-carbaldehyde, 4: POCl3 (23.46 mL, 246 mmol) was added dropwise to a stirred N,N-dimethyformamide (204 mL) at 0° C. After addition the mixture was stirred for additional 90 minutes. To the mixture was added dropwise the solution of 1-benzyl-2-methyl-1H-pyrrole, 3 (2.71 g, 45 mmol) in tetrahydrofuran (1150 mL). The reaction mixture was allowed to be stirred for 18 h from 0° C. to room temperature. The mixture was concentrated and redissolved in ethyl acetate (2 L). The mixture was washed with saturated Na2CO3 (2×500 mL). The Na2CO3 solution was extracted with ethyl acetate (7×1 L). The organic layers were combined and concentrated. The crude product was purified by silica gel chromatography (hexane to hexane:ethyl acetate, 7:1) to afford 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde, 4 as a light yellow liquid. Yield: 30.8 g (81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666898B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-156d251a788a494ea4ce7d0095a8794d
출처 메모uspto-grants-2010_02