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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111585Generated: October 30, 2026

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

https://huagongshe.com/reaction/1111585

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 one 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 numberUS04118390
Source datasetuspto-grants-1978_10
ORD IDord-ae2ad736c79a428c805c917347f338c4
Source noteuspto-grants-1978_10