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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643001Generated: November 1, 2026

(2-Methoxypyridin-3-yl)boronic acid → HCID 86614001, compound

https://huagongshe.com/reaction/643001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methoxypyridin-3-yl)boronic acidHCID 2762709—
ReactantHCID 86614002HCID 86614002—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86614001HCID 86614001—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-chloro-N-((1-(4-iodophenyl-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide (0.044 g, 0.1 mmol), 2-methoxypyridine-3-ylboronic acid (0.016 g, 0.11 mmol) and Pd(PPh3)2Cl2 (0.007 g, 0.01 mmol) in p-dioxane (0.7 mL) was purged with Argon for 5 min. A degassed aqueous solution of Na2CO3 (IM, 0.3 mL) was added. After being heated at 100° C. for 2 h, the mixture was cooled to room temperature, and purified by preparative HPLC to yield 5-chloro-N-((1-(4-(2-methoxypyridin-3-yl)phenyl-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide (MS 425.0, 427.0 (M+H), Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696352B2
Source datasetuspto-grants-2010_04
ORD IDord-26b86d36fc3447ed84e79ec30215abfa
Source noteuspto-grants-2010_04