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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 731597생성일: 2026년 10월 25일

Ammonia → 2-Oxo-2-(1H-pyrrolo[3,2-C]pyridin-3-YL)-acetamide

https://huagongshe.com/reaction/731597

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물1,4-DioxaneHCID 31275—
반응물DiisopropylethylamineHCID 81531—
반응물Npc324351HCID 3614358—
반응물3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-oneHCID 4293995—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매Sodium CarbonateHCID 10340—
생성물2-Oxo-2-(1H-pyrrolo[3,2-C]pyridin-3-YL)-acetamideHCID 22663037—

반응 단계

A mixture of methyl oxo-(1H-pyrrolo[3,2-c]-pyridin-3-yl)acetate (1 eq.) and K2CO3 (2 eq.) in methanol is stirred at room temperature for 8 h and filtered. The filtercake is air-dried to give potassium 5-azaindole 3-glyoxylate. A mixture of this glyoxylate salt, ammonia (solution in dioxane (5 eq.), 3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one (DEPBT) (1 eq.) and diisopropylethylamine (DIEA) in DMF is stirred for 8 h, diluted with EtOAc and aqueous sodium carbonate. The organic phase is separated, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified over silica gel with EtOAc/MeOH as eluent to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585876B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-84e349e9b25042308ed9039ec70ae8c1
출처 메모uspto-grants-2009_09