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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260633Generated: October 27, 2026

Sodium Hydroxide → [1-(2-Chloro-4-methanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid

https://huagongshe.com/reaction/1260633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant[1-(2-Chloro-4-methanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl esterHCID 67218985—
SolventMeOH tetrahydrofuranHCID 21899815—
Product[1-(2-Chloro-4-methanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acidHCID 11618108—

Reaction Conditions

Temperature45 °C

Reaction Steps

1M Aqueous NaOH (15 ml) is added to a stirring suspension of [1-(2-chloro-4-methanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester (2.6 g, 6.39 mmol) in 1:1 THF/MeOH (40 ml). After stirring at 45° C. for 1 hour, the reaction mixture is filtered to remove any undissolved material and is evaporated to dryness. The resulting solid is dissolved in water (30 ml) and acidified to pH 2-3 using concentrated HCl. The resulting suspension is collected by filtration and dried in vacuo at 50° C. to yield a solid which is purified by recrystallisation from IPA/water (1:3) to afford the titled product. (MH+ 393)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470848B2
Source datasetuspto-grants-2013_06
ORD IDord-bfbb0c351b9145719e23bda80355d44e
Source noteuspto-grants-2013_06