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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626969Generated: October 25, 2026

(2-Chloropyrimidin-5-yl)boronic acid → {2-[4-(Methylsulfonyl)piperidin-1-yl]pyrimidin-5-yl}boronic acid

https://huagongshe.com/reaction/626969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloropyrimidin-5-yl)boronic acidHCID 21747362—
Reactant4-(Methanesulfonyl)piperidineHCID 22275038—
Product{2-[4-(Methylsulfonyl)piperidin-1-yl]pyrimidin-5-yl}boronic acidHCID 131735244—

Reaction Steps

Prepared from 4-(methylsulfonyl)piperidine (0.515 g, 3.16 mmol) and (2-chloropyrimidin-5-yl)boronic acid (0.5 g, 3.16 mmol) in accordance with General Method C to give the title compound as an off-white semi-solid. HPLC-MS: m/z MH+ 286.2, RT 0.17 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309243B2
Source datasetuspto-grants-2016_04
ORD IDord-f3674d9d3b4c4a319438e6d541bf6878
Source noteuspto-grants-2016_04