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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764457Generated: November 2, 2026

2-(Methylamino)acetaldehyde → 2-[1-Methyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde

https://huagongshe.com/reaction/1764457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylamino)acetaldehydeHCID 13316132—
Reactant5-Bromothiazol-2-yl IsocyanateHCID 23062264—
SolventBenzeneHCID 241—
Product2-[1-Methyl-3-(5-bromothiazol-2-yl)ureido]acetaldehydeHCID 22766862—

Reaction Steps

5-Bromothiazol-2-yl isocyanate dimer (17.0 grams), benzene (70 ml) and the dimethyl acetal of 2-methylaminoacetaldehyde (13.5 grams) were charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture was then stirred at room temperature for a period of about 1 hour. After this time the reaction mixture was filtered, and the filtrate was stripped of solvent under reduced pressure, leaving an oil. This oil was chromatographed on silica gel using ethyl acetate as the diluant. The eluant was dissolved in an ethanol-water mixture and the solution was filtered. The filtrate was then stripped of solvents under vacuum to yield the desired product the dimethyl acetal of 2-[1-methyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde as a crystalline solid having a melt point of 72° to 73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116969
Source datasetuspto-grants-1978_09
ORD IDord-f83581263d174fbcb7b830d2f4cc875d
Source noteuspto-grants-1978_09