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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220397생성일: 2026년 10월 24일

Dibromomethane → 4-Bromo-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide

https://huagongshe.com/ko/reaction/220397

반응식

참여 물질

역할이름HCID투입량
반응물DibromomethaneHCID 3024—
반응물Isoamyl nitrateHCID 10985—
반응물4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamideHCID 58180503—
용매Ethyl AcetateHCID 8857—
생성물4-Bromo-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamideHCID 5818056698%

반응 조건

온도60 °C

반응 단계

A round bottom flask charged with 4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (134.4 mg, 0.397 mmol) under an atmosphere of nitrogen was treated with dibromomethane (397 μL). Isoamyl nitrate (107 μL, 0.794 mmol) was added and the reaction mixture was heated at 60° C. 3.5 h and cooled to rt. The reaction mixture was diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate. The organics were dired over anhydrous sodium sulfate, filtered and concentrated in vacuo. 4-Bromo-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (0.156 g, 0.388 mmol, 98% yield) was isolated as a brown glassy solid. The product was used immediately in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202881B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-5ed22134ef8c49759fbf0a36cf82c24e
출처 메모uspto-grants-2012_06