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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632781Generated: October 31, 2026

Toluene → tert-butyl ((3S)-1-(1-methyl-1H-pyrazol-3-yl)-5-oxopyrrolidin-3-yl)carbamate

https://huagongshe.com/reaction/632781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTributylphosphineHCID 13831—
ReactantDiethylazodicarboxylate tolueneHCID 66777355—
Reactanttert-butyl ((2S)-1-hydroxy-4-((1-methyl-1H-pyrazol-3-yl)amino)-4-oxobutan-2-yl)carbamateHCID 118065000—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl ((3S)-1-(1-methyl-1H-pyrazol-3-yl)-5-oxopyrrolidin-3-yl)carbamateHCID 11806533468.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl ((2S)-1-hydroxy-4-((1-methyl-1H-pyrazol-3-yl)amino)-4-oxobutan-2-yl)carbamate (553.0 mg) and tri-n-butylphosphine (0.924 mL) in a mixed solvent of toluene (9 mL)/THF (3 mL) was added 40% diethyl azodicarboxylate toluene solution (0.954 mL) under ice-cooling, and the mixture was stirred at 60° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (358 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321757B2
Source datasetuspto-grants-2016_04
ORD IDord-26a2ac1e81884b79b3ef80fda0371b09
Source noteuspto-grants-2016_04