Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85447Generated: October 25, 2026

5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridine → Methyl 1-isopropyl-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-indazole-4-carboxylate

https://huagongshe.com/reaction/85447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridineHCID 24208789—
ReactantMethyl 6-bromo-1-isopropyl-3-methyl-1H-indazole-4-carboxylateHCID 67466747—
ProductMethyl 1-isopropyl-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-indazole-4-carboxylateHCID 67467136—

Reaction Conditions

Temperature100 °C

Reaction Steps

The title compound was prepared in the same manner as described for example 35 (step a) from methyl 6-bromo-1-isopropyl-3-methyl-1H-indazole-4-carboxylate (1 g, 3.36 mmol) and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (0.98 g, 4.04 mmol) wherein the reaction mixture was stirred at 100° C. for 5 h. The product was collected as an off white solid (600 mg, 53%). LCMS (ES−) m/z: 333.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846935B2
Source datasetuspto-grants-2014_09
ORD IDord-3c280422e32d491da02669a4eb6bdd5e
Source noteuspto-grants-2014_09