Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169617Generated: November 1, 2026

(2-Methoxypyridin-4-yl)boronic acid → HCID 60197875, compound

https://huagongshe.com/reaction/2169617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methoxypyridin-4-yl)boronic acidHCID 23546919—
ReactantHCID 86670087HCID 86670087—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
SolventSodium BicarbonateHCID 516892—
ProductHCID 60197875HCID 60197875—

Reaction Steps

The title compound was prepared in a manner similar to EXAMPLE 1 using 2-methoxypyridin-4-ylboronic acid (270 mg, 1.765 mmol), 2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine (PREPARATION x2, 200 mg, 0.882 mmol), and PdCl2(dppf) (51.7 mg, 0.071 mmol) in dioxane (5 mL) and aqueous saturated NaHCO3 (1 mL). 1H NMR (400 MHz, DMSO-d6) δ 3.01-3.23 (m, 7 H), 3.89 (m, 3 H), 3.92-3.97 (m, 1 H), 3.99-4.06 (m, 1 H), 4.53-4.62 (m, 1 H), 7.47 (d, J=0.76 Hz, 1 H), 7.62 (s, 1 H), 7.68 (dd, J=5.31, 1.52 Hz, 1 H), 8.24 (d, J=5.56 Hz, 1 H). ESI-MS m/z [M+H]+ calc'd for C15H17N5O2, 299.14; found 300.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045496B2
Source datasetuspto-grants-2015_06
ORD IDord-f1d77177e8774120aeb077f811a0b204
Source noteuspto-grants-2015_06