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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436990Generated: October 26, 2026

2-Propargylaminoacetaldehyde → 2-[1-Propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde

https://huagongshe.com/reaction/436990

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PropargylaminoacetaldehydeHCID 20392754—
Reactant7-Bromobenzothiazol-2-yl isocyanateHCID 53646458—
SolventBenzeneHCID 241—
Product2-[1-Propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehydeHCID 20357136—

Reaction Steps

7-Bromobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-propargylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about one hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04029491
Source datasetuspto-grants-1977_06
ORD IDord-afb96df029134a9992980bcd0aa1bb36
Source noteuspto-grants-1977_06