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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201813Generated: October 28, 2026

Triethylamine → HCID 86720633, compound

https://huagongshe.com/reaction/2201813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant3-Chloro-1H-pyrrolo[3,2-c]pyridineHCID 24729215—
SolventDichloromethaneHCID 6344—
ProductHCID 86720633HCID 86720633128.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-chloro-1H-pyrrolo[3,2-c]pyridine (1 g, 6.55 mmol) in dichloromethane (10 mL), triethylamine (2.3 ml, 16.38 mmol) was added. The mixture was cooled to 0° C. and benzyl chloroformate (2.3 mL, 50% solution in dichloromethane, 9.83 mmol) was added drop wise. After complete addition, the reaction mixture was stirred at room temperature for about 1 hour. On completion, the reaction was quenched by addition of saturated aq. sodium bicarbonate solution and the organic layer was separated, washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum to afford benzyl 3-chloro-1H-pyrrolo[3,2-c]pyridine-1-carboxylate (2.42 g, 100%) as viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364466B2
Source datasetuspto-grants-2016_06
ORD IDord-5b53e8fcefdc470ba5cb978eefd3512a
Source noteuspto-grants-2016_06