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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449054Generated: October 26, 2026

4-Phenoxyphenylboronic acid → HCID 178501053, compound

https://huagongshe.com/reaction/449054

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
ReactantPotassium fluoride dihydrateHCID 23708904—
ReactantHCID 178501044HCID 178501044—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178501053HCID 178501053—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred mixture of trans-4-(8-amino-1-bromo-imidazo[1,5-a]pyrazin-3-yl)-cyclohexanecarboxylic acid methyl ester (2.00 g, 5.66 mmol) and 4-phenoxyphenylboronic acid (1.454 g, 6.7 mmol) in DME (25.00 mL) and H2O (8.3 mL) was added potassium fluoride dihydrate (1.865 g, 19.82 mmol). The mixture was bubbled with nitrogen for 5 min before Pd(PPh3)4 (330 mg, 0.28 mmol) was added to. The resulting mixture was refluxed overnight at 100° C. Solvent was removed under reduced pressure and the product was purified by flash chromatography (2% MeOH in DCM). 1H NMR (400 MHz, CD3OD) δ 1.59-1.87 (m, 4H), 2.02-2.18 (m, 4H), 2.41-2.53 (m, 1H), 3.09-3.19 (m, 1H), 3.68 (s, 3H), 6.94-7.20 (m, 6H), 7.32-7.44 (m, 2H), 7.52-7.63 (m, 3H). MS (ES+): m/z: 442.97 [MH+]. HPLC: tR=2.48 min (OpenLynx: polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481733B2
Source datasetuspto-grants-2013_07
ORD IDord-835b5df35c9044c693cd352bd7f923c4
Source noteuspto-grants-2013_07