돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1435589생성일: 2026년 10월 27일

Dimethylformamide → N-(3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl)acetamide

https://huagongshe.com/reaction/1435589

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetrahydrofuranHCID 8028—
반응물Potassium tert-butoxideHCID 23665647—
반응물N-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamideHCID 68462435—
생성물N-(3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl)acetamideHCID 6846273268%

반응 조건

온도70 °C

반응 단계

Potassium tert-butoxide (2.25 g, 20 mmol) was added to a solution of N-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamide (1.48 g, 5 mmol) in a 2:1 mixture of tetrahydrofuran and dimethylformamide (75 mL). The mixture was heated at 70° C. for 16 hours then the tetrahydrofuran was removed in vacuo. The mixture was poured onto a pad of silica and eluted with 10% methanol in ethyl acetate. The organics were concentrated in vacuo to 5% of their original volume and water (30 mL) was added. The resultant orange solid was filtered and dried to afford N-[3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)-phenyl]-acetamide (1.01 g, 68%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07618964B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-0a838b86e4f04e1d88506577eea423fd
출처 메모uspto-grants-2009_11