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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331014Generated: October 30, 2026

Cesium carbonate → tert-butyl 3-(4-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridin-1-yl)azetidine-1-carboxylate

https://huagongshe.com/reaction/331014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridineHCID 24729561—
Reactanttert-Butyl 3-(tosyloxy)azetidine-1-carboxylateHCID 57351432—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Producttert-butyl 3-(4-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridin-1-yl)azetidine-1-carboxylateHCID 8672028632.8%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a mixture of 4-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine (D6) (500 mg, 1.548 mmol) and tert-butyl 3-(tosyloxy)azetidine-1-carboxylate (D100) (558 mg, 1.703 mmol) in DMSO (10 mL) was added cesium carbonate (1513 mg, 4.64 mmol). The final mixture was heated at 80° C. for 4 hours after which the temperature is increase to 95° C. and the mixture heated overnight. The reaction mixture was diluted with water (50 mL) and then extracted with ethyl acetate (50 mL×3). The combined organics were dried over magnesium sulfate and concentrated. The crude was purified on normal phase silica eluting with ethyl acetate and cyclohexane (0-50%) to give the title compound (243 mg). LCMS (A): m/z (M+H)+ 478/480, C15H17BrIN3O2 requires 477/479 (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877742B2
Source datasetuspto-grants-2014_11
ORD IDord-40e5db476b6647cdac2ad447f4bf396b
Source noteuspto-grants-2014_11