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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924125Generated: November 2, 2026

Sodium Carbonate → 6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(pyrimidin-5-yl)nicotinamide

https://huagongshe.com/reaction/924125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
Reactant6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-iodonicotinamideHCID 86702626—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-(pyrimidin-5-yl)nicotinamideHCID 89906474—

Reaction Conditions

Temperature90 °C

Reaction Steps

6-Chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-iodonicotinamide (Stage 247.2, 8 g, 17.43 mmol), pyrimidine-5-boronic acid (4.55 g, 34.9 mmol), PdCl2(dppf) (0.638 g, 0.871 mmol), Na2CO3 (26.1 mL of 2 M, 52.3 mmol), and DME (110 mL) were added to a vial, which was sealed, evacuated/purged with argon and the RM was stirred at 90° C. for 20 h. The RM was dissolved in EtOAc (200 mL), washed with water, dried over Na2SO4 and the solvent was evaporated off under reduced pressure. The residue was purified by flash chromatography (Silica gel column, 750 g, EtOAc/n-hexane 1:1) and recrystallized from EtOAc/iPr2O to give the title product as a pink solid. HPLC (Condition 10) tR=6.77 min, UPLC-MS (Condition 3) tR=1.05 min, m/z=409.0/411.0 [M−H]−; 1H-NMR (400 MHz, DMSO-d6) δ ppm 6.59 (d, J=8.60 Hz, 2H) 7.07 (d, J=8.99 Hz, 2H) 7.75 (d, J=1.95 Hz, 1H) 8.18-8.24 (m, 1H) 8.28 (s, 2H) 8.50 (s, 1H) 9.88 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-9d6b9ef246b149d09b85a751ff11fa21
Source noteuspto-grants-2016_03