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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948082Generated: October 31, 2026

Dichloromethane → HCID 58292916, compound

https://huagongshe.com/reaction/1948082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Carboxyphenylboronic AcidHCID 312183—
ReactantHCID 58293036HCID 58293036—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58292916HCID 5829291627%

Reaction Conditions

Temperature100 °C

Reaction Steps

Diethyl[4-({4-[(7-bromo-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-4-yl)amino]-5-(trifluoromethyl)pyrimidin-2-yl}amino)-3-methoxybenzyl]phosphonate (20.0 mg, 0.0304 mmol), 4-(Dihydroxyboryl)benzoic acid (10.1 mg, 0.0608 mmol), potassium carbonate (12.6 mg, 0.0911 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (1:1) (2.48 mg, 0.00304 mmol), 1,4-dioxane (0.6 mL) and water (0.15 mL) were mixed and heated in microwave at 100° C. for 30 minutes. The crude mixture was passed through Thiol-SPE cartridge to remove Pd and was subsequently purified by MDP to obtain the title compound (5.7 mg, 27% yield). 1H NMR (400 MHz, DMSO-d6) δ=1.13 (t, J=7.1 Hz, 6H), 3.08 (s, 3H), 3.34 (d, J=21.5 Hz, 2H), 3.75 (s, 3H), 3.85-4.02 (m, 4H), 4.67 (s, 2H), 6.94 (d, J=8.1 Hz, 1H), 7.08 (br. s., 1H), 7.43 (br. s., 1H), 7.58 (d, J=8.6 Hz, 1H), 7.75 (m, J=8.3 Hz, 2H), 8.02 (m, J=8.6 Hz, 2H), 8.42 (s, 1H), 9.20 (s, 1H), 13.05 (s, 1H). MS (ES+): m/z 700.25 (100) [MH+]; HPLC: tR=1.07 min (UPLC, purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-95bfda8800e24b89b47ccac4c1673a93
Source noteuspto-grants-2013_03