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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593507Generated: November 2, 2026

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

https://huagongshe.com/reaction/1593507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,4-DioxaneHCID 31275—
ReactantDiisopropylethylamineHCID 81531—
ReactantNpc324351HCID 3614358—
Reactant3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-oneHCID 4293995—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product2-Oxo-2-(1H-pyrrolo[3,2-C]pyridin-3-YL)-acetamideHCID 22663037—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297705B2
Source datasetuspto-grants-2007_11
ORD IDord-15bacb3c26e2490a91515fb0c756cb72
Source noteuspto-grants-2007_11