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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923946Generated: October 30, 2026

Water → HCID 89906673, compound

https://huagongshe.com/reaction/923946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
ReactantHCID 89906996HCID 89906996—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 89906673HCID 89906673—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Bromo-3-iodo-N-(4-(trifluoromethoxy)phenyl)benzamide (Stage 117.2, 3 g, 6.17 mmol), pyrimidin-5-ylboronic acid (841 mg, 6.79 mmol), Pd(PPh3)2Cl2 (217 mg, 0.309 mmol) and Na2CO3 (1.963 g, 18.52 mmol) in a mixture of DME (17.28 mL), water (4.94 mL), EtOH (2.469 mL) was degassed and stirred at 80° C. for 23 h under argon. Additional pyrimidin-5-ylboronic acid (76 mg, 0.613 mmol) was added to the RM and stirring was continued for 5 h. The RM was treated with Si-Thiol (Silicycle, 1.27 mmol/g, 1.215 g, 1.543 mmol), filtered and the filtrate was evaporated off under reduced pressure to give a residue which was purified by flash chromatography (Silica gel column, 80 g, cyclohexane/EtOAc, from 10% to 45% EtOAc) to yield the title compound as a white crystalline solid. UPLC-MS (condition 1) tR=2.80 min, m/z=437.9-439.9 [M+H]+, m/z=436.0-438.0 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-d4d0305ff1ca4e879880d0c08bfd47ef
Source noteuspto-grants-2016_03