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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046261Generated: October 26, 2026

Sodium Carbonate → 3-{(S)-1-[4-(1-Cyclopropyl-1H-pyrazol-4-yl)-phenyl]-ethyl}-(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-[1,3]oxazinan-2-one

https://huagongshe.com/reaction/1046261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-1-isopropyl-1H-pyrazoleHCID 22329200—
Reactant(S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-2-oneHCID 59532385—
SolventDimethylformamideHCID 6228—
Product3-{(S)-1-[4-(1-Cyclopropyl-1H-pyrazol-4-yl)-phenyl]-ethyl}-(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-[1,3]oxazinan-2-oneHCID 58485376—

Reaction Conditions

Temperature90 °C

Reaction Steps

2 M aqueous Na2CO3 solution (0.37 mL) was added to a solution of 4-bromo-1-isopropyl-1H-pyrazole (0.15 g) and (S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-[(S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl]-1,3-oxazinan-2-one (0.35 g) in dimethylformamide (3 mL). The resulting mixture was sparged with argon for 10 min, before [1,1′-bis(diphenylphosphino)-ferrocene]dichloro-palladium(II) dichloromethane complex (20 mg) was added. The mixture was heated to 90° C. and stirred at this temperature for 2 h. After cooling to ambient temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4), and concentrated. The residue was purified by chromatography on silica gel (tert-butyl methyl ether/dichloromethane/NH4OH 96:4:0.1->94:6:0.1) to afford the title compound as a solid. Yield: 0.18 g (55% of theory); Mass spectrum (ESI+): m/z=460 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-c8c9b9fd1821464fb5d5afd6c0d733fe
Source noteuspto-grants-2013_10