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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348033Generated: November 1, 2026

Potassium Carbonate → HCID 10091401, compound

https://huagongshe.com/reaction/348033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant2-(2-Chlorophenyl)-7-ethoxy-3-iodopyrazolo[1,5-a]pyrimidineHCID 21083701—
ProductHCID 10091401HCID 1009140129.3%

Reaction Conditions

Temperature87 °C

Reaction Steps

To a mixture of 2-(2-chlorophenyl)-7-ethoxy-3-iodopyrazolo[1,5-a]pyrimidine (1–11A-1a; 6.76 g, 16.9 mmol), 4-chlorophenylboronic acid (4.07 g, 26.0 mmol), powdered K2CO3 (4.7 g, 34 mmol) and (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium(II), dichloromethane complex (0.69 g, 0.85 mmol) was added degassed dimethoxyethane (136 ml) and water (34 ml). The reaction was heated at 87° C. for 1.5 hours, cooled, and then concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with 1 M aqueous NaOH, 1 M aqueous HCl, and brine. Suspended solids were collected by filtration (3.0 g). The solvent was removed, in vacuo, and the residue was triturated from ethanol to give additional solids (1.9 g). The combined solids were purified by silica gel chromatography using 9:1 methylene chloride/ hexanes as eluant to afford 11A-1 (4.45 g, 68%) as an off-white solid: +ESI MS (M+1) 384.3; 1H NMR (400 MHz, CD3OD) δ 8.51 (d, J=5.0 Hz, 1H), 7.53–7.40 (m, 6H), 7.24 (d, J=8.7 Hz, 2H), 6.66 (d, J=5.0 Hz, 1H), 4.59 (q, J=7.1 Hz, 2H), 1.60 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176210B2
Source datasetuspto-grants-2007_02
ORD IDord-d9fcd9aa192345aaa38476a81007f129
Source noteuspto-grants-2007_02