Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054389Generated: November 3, 2026

Sodium Carbonate → HCID 135974539, compound

https://huagongshe.com/reaction/2054389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant7-(2-Chlorophenyl)-8-iodo-2-methyl-3H-pyrazolo[1,5-a][1,3,5]triazin-4-oneHCID 135974537—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 135974539HCID 135974539—

Reaction Steps

To a mixture of 7-(2-chlorophenyl)-8-iodo-2-methyl-3H-pyrazolo-[1,5-a][1,3,5]triazin-4-one (I-1A-1d; 141 g, 364 mmol) and 4-chlorophenylboronic acid (85.1 g, 544 mmol) in dimethoxyethane (1.4 L) was added 2 M aqueous Na2CO3 (365 ml) and then (1,1′-bis(diphenylphosphino)ferrocene)-dichloropalladium(II), dichloromethane complex (5.80 g, 7.17 mmol). The reaction was heated at reflux for 16 hours, cooled, and the organic layer separated and then concentrated under reduced pressure. The residue was dissolved in methyltetrahydrofuran (1.4 L) and washed with 1 M aqueous NaOH (2×700 ml) and 1 M aqueous HCl (700 ml). The solvent was removed, in vacuo, to give a brown solid which was suspendend in methanol (1.2 L). The mixture was concentrated to one-third volume, the solids were collected by vacuum filtration in a course sintered glass funnel, washed with methanol (1 L) and then dried, in vacuo, to afford product I-2A-1a as a light-brown solid (103 g, 76%): +APcI MS (M+1) 371.3; 1H NMR (400 MHz, DMSO-d6) δ 12.73 (s, 1H), 7.54-7.43 (m, 4H), 7.35-7.26 (m, 4H), 2.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329658B2
Source datasetuspto-grants-2008_02
ORD IDord-941fc390f95a40038b8f186c02e445a5
Source noteuspto-grants-2008_02