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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230590Generated: November 1, 2026

L-Threonine → Ethyl5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoate

https://huagongshe.com/reaction/230590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ThreonineHCID 6288—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
ReactantMethyl 5-acetyl-2-[(methylsulfonyl)amino]benzoateHCID 66978055—
SolventTetrahydrofuranHCID 8028—
SolventTitanium tetraethoxideHCID 76524—
ProductEthyl5-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-[(methylsulfonyl)amino]benzoateHCID 5776293023%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of methyl 5-acetyl-2-[(methylsulfonyl)amino]benzoate (13.2 g, 49 mmol, PCT Int. Appl. WO2005003084) in titanium (IV) ethoxide (100 ml) and tetrahydrofuran (THF) (100 ml) was added (R)-(+)-2-methylpropane-2-sulfinamide (5.9 g, 49 mmol, Advanced Asymmmetry) and the mixture was stirred for 16 hours at 80° C. The mixture was cooled to room temperature and then to 0° C. before it was added dropwise into a 0° C. solution of sodium borohydride (7.4 g, 195 mmol). Thre mixture was stirred at 0° C. for 3 hours and then warmed to room temperature. The reaction was quenched with methanol and stirred for 30 minutes. Water was added to the mixture and it was stirred for 10 minutes. The resulting suspension was filtered through a pad of Celite and the filter cake was washed with ethyl acetate. The filtrate was concentrated under reduced pressure to give the residue, which was applied to a silica gel chromatography column and eluted with a volume mixture of dichloromethane and ethyl acetate (1:1) to furnish 4.3 g (23% yield) of the title compound as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566739B2
Source datasetuspto-grants-2009_07
ORD IDord-495160335735484182ccb75216961d8a
Source noteuspto-grants-2009_07