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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827999Generated: October 26, 2026

Methanesulfonyl chloride → Ethyl 2-((diphenylmethylene)amino)-2-(pyrazin-2-yl)acetate

https://huagongshe.com/reaction/1827999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
ReactantSodiumHCID 5360545—
Reactant(4-(Phenoxymethyl)phenyl)methanolHCID 11333367—
ReactantPyrazin-2-ylmethyl methanesulfonateHCID 15096999—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-((diphenylmethylene)amino)-2-(pyrazin-2-yl)acetateHCID 1024697178%

Reaction Steps

A solution of 2-(methanesulfonyloxymethyl)pyrazine (5 mmole), (prepared from 2′-(pyrazin-2-yl)styrene according to the procedure in EP 02257, followed by treatment with methanesulfonyl chloride, according to a procedure in Can. J. Chem. 1999, 77 (4) 463 in 20 ml THF was added dropwise to the sodium salt of ethyl N-(diphenylmethylene)glycinate (5 mmole) in 20 ml DMF cooled in an ice bath. The mixture was allowed to warm to room temperature during 4 hrs. The reaction mixture was partitioned between ether and water. The aqueous layer was separated and reextracted with ether (75 ml). The combined ethereal extracts were washed with brine and dried over MgSO4. Evaporation of the solvent afforded a residue which was chromatographed on silica and eluted with acetone:hexane (1:3) to afford 1.27 g (78%) of ethyl 2-(pyrazin-2-yl)-N-(diphenylmethylene)glycinate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056903B2
Source datasetuspto-grants-2006_06
ORD IDord-adc600777d324d9998abf328ccfeb6d9
Source noteuspto-grants-2006_06