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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40861Generated: October 27, 2026

Citric Acid → Benzyl 1H-pyrrolo[2,3-b]pyridin-5-ylcarbamate

https://huagongshe.com/reaction/40861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant1H-pyrrolo(2,3-b)pyridin-5-amineHCID 11715187—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 1H-pyrrolo[2,3-b]pyridin-5-ylcarbamateHCID 5941452577%

Reaction Conditions

Temperature0 °C

Reaction Steps

1H-pyrrolo[2,3-b]pyridin-5-amine (9.45 g, 71.05 mmol) was dissolved in THF (150 mL) and stirred at 0° C. under an atmosphere of nitrogen. Benzyl chloroformate (20.3 mL, 142.10 mmol, 2.0 Eq) was added dropwise over a period of 15 minutes and the mixture allowed to stir at room temperature for 30 minutes. The mixture was treated with 4M NaOH (aq) (53.3 mL, 213.16 mmol, 3.0 Eq) over a period of 15 minutes and the resultant brown solution left to stir for 16 hours. The reaction mixture was taken to pH 4 (125 mL of 10% aq. citric acid) and the 2 layers were separated. The aqueous layer was back extracted with EtOAc and the combined organics were dried over magnesium sulphate, filtered and dried under vacuum. The crude product was purified by column chromatography (50% EtOAc/Petroleum Ether) to give 14.59 g (77%) of pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530489B2
Source datasetuspto-grants-2013_09
ORD IDord-ae19c2d4d4fc4ea2b33189d88344e62e
Source noteuspto-grants-2013_09