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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396361Generated: November 2, 2026

1H-Pyrrolo(2,3-b)pyridine → HCID 178526243, compound

https://huagongshe.com/reaction/1396361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
Reactantm-Chloroperbenzoic acidHCID 70297—
SolventEthyl AcetateHCID 8857—
ProductHCID 178526243HCID 178526243—

Reaction Conditions

Temperature0 °C

Reaction Steps

1H-pyrrolo[2,3-b]pyridine (2.8 g, 24 mmol) was dissolved in ethyl acetate (24 mL) and cooled to 0° C. A solution of 3-chloroperbenzoic acid (77%, 6.7 g, 30.1 mmol) in ethyl acetate (24 mL) was added drop-wise then the reaction mixture warmed to 25° C. over 16 h. The reaction mixture was cooled to 0° C., filtered, and the solids dried to give crude 1H-pyrrolo[2,3-b]pyridine 7-oxide, 3-chlorobenzoic acid complex (4.1 g, 58%) as an off-white solid. This was used directly in the next step without purification. LCMS (EI/CI) m/z: 135 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901124B2
Source datasetuspto-grants-2014_12
ORD IDord-f24c7f49a97247b1af511e3a94b25ea8
Source noteuspto-grants-2014_12