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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083613Generated: October 29, 2026

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

https://huagongshe.com/reaction/2083613

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 numberUS04086240
Source datasetuspto-grants-1978_04
ORD IDord-484cf374a70d467bb1899681c3718435
Source noteuspto-grants-1978_04