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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853487Generated: October 31, 2026

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

https://huagongshe.com/reaction/1853487

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 numberUS08962642B2
Source datasetuspto-grants-2015_02
ORD IDord-9d06cb307cf041468fb4e1e2567f98e3
Source noteuspto-grants-2015_02