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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261612Generated: November 3, 2026

Acetate → 1-(3-Hydroxy-pyrrolo[2,3-b]pyridin-1-yl)-ethanone

https://huagongshe.com/reaction/2261612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantSodiumHCID 5360545—
ReactantHCID 49845771HCID 49845771—
SolventMethanolHCID 887—
Product1-(3-Hydroxy-pyrrolo[2,3-b]pyridin-1-yl)-ethanoneHCID 59593336—

Reaction Steps

1-(3-Hydroxy-pyrrolo[2,3-b]pyridin-1-yl)-ethanone 503 is prepared from acetic acid 1-acetyl-1H-pyrrolo[2,3-b]pyridin-3-yl ester 502 by selective removal of the acetate at the 3-position by reaction with sodium in methanol at room temperature typically for 30 minutes to one hour, followed by purification and isolation by conventional means (e.g. extraction and recrystallization).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846941B2
Source datasetuspto-grants-2010_12
ORD IDord-18025229fabc4922b8e930423510028b
Source noteuspto-grants-2010_12