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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523472Generated: October 30, 2026

Water → methyl 5-chloro-1-(4-fluorobutyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/523472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-4-fluorobutaneHCID 10022—
ReactantCesium carbonateHCID 10796—
Reactantmethyl 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylateHCID 84677991—
SolventDimethylformamideHCID 6228—
Productmethyl 5-chloro-1-(4-fluorobutyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylateHCID 86698873—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylate 11-c (2.9 g, 12.2 mmol) in DMF (50 mL) were added successively cesium carbonate (4 g, 12.2 mmol) and 1-bromo-4-fluorobutane (1.3 mL, 12.2 mmol). The resulting mixture was heated at 60° C. overnight. The reaction mixture was allowed to cool down to room temperature then poured into iced water and the product was extracted 3 times with DCM. The combined organic layers were dried over Na2SO4, filtered and evaporated to give the targeted product 11-d as a yellowish solid. The product was used as such in the next step. m/z=313 (M+H)+, Cl pattern.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339494B2
Source datasetuspto-grants-2016_05
ORD IDord-3bbaad259d6d4d30ad53f4ca345f1d3c
Source noteuspto-grants-2016_05