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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114508Generated: October 30, 2026

3-Pyridinylboronic acid → HCID 59809563, compound

https://huagongshe.com/reaction/2114508

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantN-[2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamideHCID 3843065—
ReactantHCID 11516034HCID 11516034—
ReactantHCID 59809550HCID 59809550—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59809563HCID 59809563—

Reaction Steps

Using an adaptation of the method described in Procedure 16, substituting 4-(3-chloro-phenoxazin-10-yl)-piperidine-1-carboxylic acid tert-butyl ester, 2i, for 3-bromo-10-piperidin-4-yl-10H-phenothiazine, 5e, N-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetamide for 3-pyridyl boronic acid, Cp2Fe(PtBu2)2PdCl2 for Pd(PPh3)4 and a 5:1 mixture of dioxane:water for NMP, the title compound 4-[3-(2-acetylaminophenyl)-phenoxazin-10-yl]-piperidine-1-carboxylic acid tert-butyl ester, 1j was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432257B2
Source datasetuspto-grants-2008_10
ORD IDord-5f76ec13d8464d0a8d46cddb6f89d109
Source noteuspto-grants-2008_10