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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157175Generated: November 2, 2026

2-Bromopyrimidine → 4-Pyrimidin-2-ylethynyl-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1157175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyrimidineHCID 78345—
Reactanttert-Butyl 4-ethynylpiperidine-1-carboxylateHCID 15550481—
CatalystHCID 178418476HCID 178418476—
Product4-Pyrimidin-2-ylethynyl-piperidine-1-carboxylic acid tert-butyl esterHCID 669398778%

Reaction Steps

To a suspension of 2-bromopyrimidine (175 mg, 1.1 mmols), dichlorobis(triphenylphosphine)palladium(II) (35 mg, 0.05 mmols) and Cul (10 mg, 0.05 mmols) was added a solution of 4-ethynyl-piperidine-1-carboxylic acid tert-butyl ester (209 mg, 1 mmol). The mixture was stirred overnight, filtered through Celite, concentrated. The residue was partitioned between ethyl acetate and water, organic layer was isolated, dried (MgSO4), and concentrated. The residue was chromatographed on silica gel eluting with ethyl acetate in hexanes (1:1) to give un-reacted 2-bromopyrimidine (130 mg), then the title compound (23 mg). LCMS m/e (288, M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807672B2
Source datasetuspto-grants-2010_10
ORD IDord-695b4f25884544aaada8ec2d8911a5bc
Source noteuspto-grants-2010_10