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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892559Generated: November 1, 2026

3-(Dimethylamino)acrylaldehyde → 2-methyl-N-(3-(pyrimidin-2-yl)oxetan-3-yl)propane-2-sulfinamide

https://huagongshe.com/reaction/1892559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Dimethylamino)acrylaldehydeHCID 638320—
ReactantSodium MethoxideHCID 10942334—
Reactant3-(1,1-Dimethylethylsulfinamido)oxetane-3-carboximidamideHCID 67957884—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product2-methyl-N-(3-(pyrimidin-2-yl)oxetan-3-yl)propane-2-sulfinamideHCID 67958161—

Reaction Steps

To a yellow solution of 3-(1,1-dimethylethylsulfinamido)oxetane-3-carboximidamide (crude from above, assumed 0.494 mmol) in MeOH (2 ml) in a 50 ml sealed tube was added (E)-3-(dimethylamino)acrylaldehyde (0.090 g, 0.912 mmol), and the reaction mixture stirred for 10 min. Sodium methoxide (0.43 ml, 1.824 mmol, 25 wt % in MeOH) was added to the mixture, which was then stirred at 65° C. for overnight. The reaction mixture was diluted with ethyl acetate and washed with water. The aqueous layer was back extracted with ethyl acetate (3×25 ml). The combined organic layers was washed with saturated brine solution, dried over Na2SO4, filtered and concentrated. The crude material was purified by pre-HPLC. Overall yield of two steps: (30 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507683B2
Source datasetuspto-grants-2013_08
ORD IDord-ade5faed7d97427db8d7ad7715939420
Source noteuspto-grants-2013_08