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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510187Generated: October 30, 2026

Dimethyl Sulfoxide → tert-butyl (2R)-2-[(6-chloropyrazin-2-yl)amino]propanoate

https://huagongshe.com/reaction/510187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant2,6-DichloropyrazineHCID 78504—
ReactantDiisopropylethylamineHCID 81531—
ReactantD-Alanine tert-butyl ester hydrochlorideHCID 16211919—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (2R)-2-[(6-chloropyrazin-2-yl)amino]propanoateHCID 117639895—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a reaction vessel was added 2,6-dichloropyrazine (CA, 492 mg, 3.30 mmol), D-Alanine tert-butyl ester hydrochloride (Aldrich Chemical) (500 mg, 2.75 mmol), DMSO (3 mL) and DIPEA (1.923 mL, 11.01 mmol). The resulting solution was heated to 120° C. for 18 hrs. The reaction mixture was cooled and diluted with ethyl acetate (30 mL). The organic layer was washed with aqueous sodium hydrogen carbonate followed by aq. brine. The aqueous layers were back extracted with ethyl acetate and the combined organic layers dried with sodium sulfate, filtered and concentrated to give an oil. The residue was purified by silica gel chromatography on Biotage 50 g SNAP column, eluting with EtOAc/Hexane (10-60%) to give the product, I-9, as a yellow oil. (663 mg, 93%) LRMS (ESI) m/z 258.1 [(M+H)+; calcd for C11H16ClN3O2: 258.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096598B2
Source datasetuspto-grants-2015_08
ORD IDord-03b90a0008384bc4902bf7f67259f55a
Source noteuspto-grants-2015_08