Reaktion #1831493

Reaktionsgleichung

5-Bromo-3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione

5-bromo-3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione

2-fluoro-3-methoxyphenylboronic acid

→

compound 11c

Ausbeute 32.3%

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

Ausbeute 32.3%

Lösungsmittel

EtOH ethylene glycol dimethyl ether

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction mixture was deoxygenated with N2 for 10 minutes
2. 2
   SonstigeThe reaction mixture was partitioned between brine and EtOAc
3. 3
   TrocknenThe organic layer was dried (sodium sulfate)
4. 4
   Sonstigeevaporated
5. 5
   Sonstigepurified by flash chromatography (silica, 30% EtOAc/hexanes)

Vorschrift

5-Bromo-3-[2(R)-tert-butoxycarbonylamino-2-cyclohexylethyl]-1-[2,6-difluorobenzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione 11b (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(triphenylphosphine) 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 11c (348 mg, 32.3%). MS (CI) m/z 502.2 (MH+−Boc).

Quelle