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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866713Generated: October 28, 2026

HCID 140533337, compound → 1-Benzyl 2-methyl (2R)-2-[(3S)-3-{[(S)-tert-butylsulfinyl]amino}-3-(3,5-difluorophenyl)propyl]pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1866713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 140533337HCID 140533337—
ReactantHCID 178505930HCID 178505930—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl 2-methyl (2R)-2-[(3S)-3-{[(S)-tert-butylsulfinyl]amino}-3-(3,5-difluorophenyl)propyl]pyrrolidine-1,2-dicarboxylateHCID 86625745—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a stirred solution of 1-benzyl 2-methyl(2R)-2-((3E)-3-{[(S)-tert-butylsulfinyl]imino}propyl)pyrrolidine-1,2-dicarboxylate from Step B (1.56 g, 3.70 mmol) in toluene (30 mL) at −78° C. was added 3,5-difluorophenylmagnesium bromide (14.8 mL of a 0.5 M solution in THF, 7.41 mmol) dropwise. The reaction mixture was stirred for 30 min at −78° C., 3.5 h at −10° C., and then at ambient temperature for 1.5 h. The mixture was quenched with saturated aqueous NH4Cl (50 mL) and extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine (30 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—95:5 to 0:100, to give the title compound. MS: m/z=537 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629338B2
Source datasetuspto-grants-2009_12
ORD IDord-604cb5fea0454b5bb052b159b8e738bb
Source noteuspto-grants-2009_12