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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335144Generated: October 29, 2026

Water → ethyl 5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate N-oxide

https://huagongshe.com/reaction/335144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantethyl 5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylateHCID 18953634—
SolventDichloromethaneHCID 6344—
Productethyl 5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate N-oxideHCID 6699505574%

Reaction Steps

mCPBA (7.3 g, 30 mmol) was added into a solution of ethyl 5H-pyrrolo[3,4-b]pyridine-6(7H)-carboxylate (5 g, 26 mmol) in CH2Cl2 (200 mL) and stirred for 2 hours. The reaction was poured into water and extracted with CH2Cl2. The organic layer was washed with aqueous sodium bisulfate, NaHCO3 and brine, dried with Na2SO4, filtered and concentrated to afford the title compound (4 g, 74% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883828B2
Source datasetuspto-grants-2014_11
ORD IDord-15ed5a4d79264b83ae2a2f7429a56439
Source noteuspto-grants-2014_11