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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404291Generated: November 1, 2026

3-Bromo-5-iodopyridine → HCID 66653094, compound

https://huagongshe.com/reaction/1404291

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-iodopyridineHCID 820409—
ReactantTripotassium phosphate trihydrateHCID 18407952—
Reactanttert-butyl 4-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylateHCID 45480279—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66653094HCID 66653094—

Reaction Conditions

Temperature80 °C

Reaction Steps

A slurry of 2.50 g (8.81 mmol) 3-bromo-5-iodo-pyridine, 3.66 g (9.7 mmol) 4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-piperidin-1-carboxylic acid tert.butyl ester (synthesis described in WO 2007/066187) and 3.74 g (17.6 mmol) tri-potassium-phosphate-trihydrate in 30 ml 1,2-dimethoxyethane was heated to 80° C. under nitrogen. Then 618 mg (0.88 mmol) bis-(triphenylphosphine)-palladium(II)-chloride were added. The reaction mixture was stirred for 16 hours at 80° C. The reaction mixture was partitioned between THF and brine. The organic phase was dried over sodium sulfate and evaporated yielding 4-[4-(5-bromo-pyridin-3-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl-ester as slightly yellow crystals; HPLC-MS: 2.28 min, [M+H] 407/409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912216B2
Source datasetuspto-grants-2014_12
ORD IDord-ecfd782f5063487889a4131413284e0b
Source noteuspto-grants-2014_12