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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216977Generated: October 31, 2026

Potassium Carbonate → (S)-tert-Butyl 4-(1-amino-3-(4-(2-methyl-1-oxoisoindolin-5-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-tert-Butyl 4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568595—
Reactant(2-Methyl-1-oxoisoindolin-5-yl)boronic acidHCID 59568610—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(S)-tert-Butyl 4-(1-amino-3-(4-(2-methyl-1-oxoisoindolin-5-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 5956858387.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Potassium carbonate (276 mg) in water (2.0 mL) was added to (S)-tert-butyl 4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 1, step (iii), 517 mg), 2-methyl-1-oxoisoindolin-5-ylboronic acid (Example 31, step (iii), 191 mg) and 1,1 bis(di-tert-butylphosphino)ferrocene palladium dichloride (98 mg) in degassed acetonitrile (12 mL) at 20° C. under nitrogen. The resulting solution was stirred at 80° C. for 30 min. The reaction mixture was cooled, filtered and diluted with dichloromethane, and washed with water. The organic extract was dried over magnesium sulfate, filtered and evaporated to afford crude product. The crude product was purified by chromatography in silica eluting with methanol/ethyl acetate (5:95 to 15:85). Pure fractions were evaporated to dryness to afford the sub-titled compound (469 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193239B2
Source datasetuspto-grants-2012_06
ORD IDord-5779731748a2488eb60f2027d732712c
Source noteuspto-grants-2012_06