Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951226Generated: November 4, 2026

N,N-Dimethyl-beta-alaninamide → 3-{3-[5-(2,6-Dimethyl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-ureido}-N,N-dimethyl-propionamide

https://huagongshe.com/reaction/1951226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-beta-alaninamideHCID 12742480—
ReactantImidazole-1-carboxylic acid [5-(2,6-dimethyl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-amideHCID 86610333—
SolventDimethylformamideHCID 6228—
Product3-{3-[5-(2,6-Dimethyl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-ureido}-N,N-dimethyl-propionamideHCID 11291391—

Reaction Steps

To a stirred solution of imidazole-1-carboxylic acid [5-(2,6-dimethyl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-amide (Intermediate BA) (0.05 g, 0.16 mmol) in DMF (1.5 ml) under an inert atmosphere is added 3-amino-N,N-dimethyl-propionamide (Amine) (0.018 g, 0.16 mmol). The reaction mixture is stirred at room temperature for 18 hours. The solvent is removed in vacuo and the resulting crude residue is dissolved in THF and passed through a plug of polymer supported isocyanate resin (0.5 g, pre-washed with THF). The solution is concentrated in vacuo and the crude residue is trituated with ether-ethyl acetate to afford the titled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404684B2
Source datasetuspto-grants-2013_03
ORD IDord-dc7d044396cb4061bbc5120b444a773b
Source noteuspto-grants-2013_03