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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402596Generated: October 25, 2026

Potassium tert-butoxide → 5-Chloro-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/402596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5-Chloro-3-((trimethylsilyl)ethynyl)pyridin-2-amineHCID 24729465—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium chloride; waterHCID 57417360—
Product5-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 24229213—

Reaction Conditions

Temperature80 °C

Reaction Steps

Under a nitrogen atmosphere, to a solution of potassium tert-butoxide (4.0 g, 0.036 mol) in 1-methyl-2-pyrrolidone (8.0 mL) which stirred with heating at 80° C., a solution of 2-amino-5-chloro-3-[(trimethylsilyl)ethynyl]pyridine (4.0 g, 0.018 mol) in 1-methyl-2-pyrrolidone (22 mL) was added dropwise and the mixture was stirred for 1 h. Cooled to ambient temperature, the reaction mixture was diluted with brine and stirred, then extracted with diethyl ether for 3 times. The organic layer was washed with brine, dried over sodium sulfate and concentrated to afford 5-chloro-7-azaindole as solid (2.3 g, y. 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-1c9338128f2b4d4896b90c169b620e39
Source noteuspto-grants-2014_06