Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054523Generated: October 30, 2026

2-Fluoro-3-methoxyphenylboronic acid → 3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-5-(2-fluoro-3-methoxyphenyl)-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/2054523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-3-methoxyphenylboronic acidHCID 4985744—
Reactant5-bromo-3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dioneHCID 21018402—
SolventDimethoxyethane ethanolHCID 20074477—
Product3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-5-(2-fluoro-3-methoxyphenyl)-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dioneHCID 5896500632.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Bromo-3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione 2b (1.0 g, 1.79 mmol) in bezene/EtOH/ethylene glycol dimethyl ether (20/2/22 mL) was added 2-fluoro-3-methoxyphenylboronic acid (382 mg, 2.24 mmol) and saturated Ba(OH)2/water (˜0.5 M, 15 mL). The reaction mixture was deoxygenated with N2 for 10 minutes, tetrakis(triphenylphosine) palladium (0) (208 mg, 0.18 mmol) was added and the reaction mixture was heated at 80° C. overnight under N2. The reaction mixture was partitioned between brine and EtOAc. The organic layer was dried (sodium sulfate), evaporated, and purified by flash chromatography (silica, 30% EtOAc/hexanes) to give compound 2c (348 mg, 32.3%). MS (CI) m/z 502.20 (MH+-Boc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329669B2
Source datasetuspto-grants-2008_02
ORD IDord-da5ef2d7a6f2438895703209094e96d5
Source noteuspto-grants-2008_02