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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616241Generated: November 1, 2026

Dimethylformamide → HCID 77230824, compound

https://huagongshe.com/reaction/1616241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 54297327HCID 54297327—
ReactantHCID 77230825HCID 77230825—
SolventEthyl AcetateHCID 8857—
ProductHCID 77230824HCID 77230824—

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Chloro-N-(prop-2-en-1-yl)pyridine-2,3-diamine (71-3, 9.52 g, 51.8 mmol, 1.0 equiv) was added to anhydrous DMF (55 mL) to give a dark purple solution. Bis(2,5-dioxocyclopentyl)carbonate (13.18 g, 51.8 mmol, 1.0 equiv) was added in one portion to give a dark green solution. The resulting reaction mixture was then heated to 80° C. After 18 h, the reaction contents were cooled to RT, diluted with EtOAc (100 mL) and added slowly to saturated aqueous NaHCO3 (200 mL). The layers were separated and the aqueous layer was back-extracted with 3×100 mL EtOAc. The combined organics were dried over Na2SO4, filtered and concentrated to give a dark purple residue. Purification by normal-phase HPLC provided 5-chloro-3-(prop-2-en-1-yl)-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (71-4) as a tan solid. LRMS (M+H)+: observed=210.0, calculated=209.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765784B2
Source datasetuspto-grants-2014_07
ORD IDord-8e65bc3bbccc4c9bace9dbb5e516f2b5
Source noteuspto-grants-2014_07