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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dibromomethane | HCID 3024 | — |
| 반응물 | Isoamyl nitrate | HCID 10985 | — |
| 반응물 | 4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide | HCID 58180503 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-Bromo-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide | HCID 58180566 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08202881B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-5ed22134ef8c49759fbf0a36cf82c24e |
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| 출처 메모 | uspto-grants-2012_06 |
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