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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284564Generated: October 25, 2026

Triethylamine → tert-butyl 6-bromo-1H-pyrazolo[4,3-b]pyridine-1-carboxylate

https://huagongshe.com/reaction/2284564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant6-Bromo-1H-pyrazolo[4,3-b]pyridineHCID 40152259—
Reactanttert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylateHCID 50986454—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
Producttert-butyl 6-bromo-1H-pyrazolo[4,3-b]pyridine-1-carboxylateHCID 8671547293%

Reaction Steps

Analogous to the preparation of tert-butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate, 6-bromo-1H-pyrazolo[4,3-b]pyridine (2.0 g, 10.10 mmol) was reacted with di-tert-butyl dicarbonate (2.8 g, 13.10 mmol), NEt3 (1.44 g, 2.0 mL, 14 mmol) and 4-(dimethylamino)pyridine in acetonitrile (20 mL) for 3 h. Work-up as discussed previously in the preparation of tert-butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate provided desired product of tert-butyl 6-bromo-1H-pyrazolo[4,3-b]pyridine-1-carboxylate as a brown solid (2.8 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145433B2
Source datasetuspto-grants-2015_09
ORD IDord-5aab59fe29124a0b8ad8dbb22356177a
Source noteuspto-grants-2015_09