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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171004Generated: October 30, 2026

Triethylamine → HCID 66653094, compound

https://huagongshe.com/reaction/2171004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
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 suspension of 5.68 g (20.0 mmol) 3-bromo-5-iodo-pyridine, 7.55 g (20.0 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 8.49 g (40.0 mmol) tri-potassium-phosphate-trihydrate in 40 ml 1,2-dimethoxyethane was heated to 80° C. under nitrogen. Then 421 mg (0.60 mmol) bis-(triphenylphosphine)-palladium(II)-chloride and 50 μl (0.361 mmol) triethylamine were added. The reaction mixture was stirred for 16 hours at 80° C. The reaction mixture was partitioned between THF and saturated sodium chloride solution. The organic phase was dried over sodium sulfate and evaporated. The residue was recrystallized from isopropanol yielding 4-[4-(5-bromo-pyridin-3-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl-ester as slightly yellow crystals; HPLC-MS (A): 2.41 min, [M+H] 407/409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051318B2
Source datasetuspto-grants-2015_06
ORD IDord-17d8b98318d849b9aebb904652092af6
Source noteuspto-grants-2015_06