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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649297Generated: October 26, 2026

Aziridine → N-cyano-N'-methyl-1-aziridinoamidine

https://huagongshe.com/reaction/649297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAziridineHCID 9033—
ReactantHCID 13186920HCID 13186920—
SolventAcetonitrileHCID 6342—
ProductN-cyano-N'-methyl-1-aziridinoamidineHCID 1315095677%

Reaction Steps

N-Cyano-N'-methyl-O-phenylisourea (0.471 g, 2.69 mmol) was added during 2 minutes to aziridine (0.521 g, 12.1 mmol) at 20° with stirring. Immediate solution occurred, some heat was evolved, and after 5 min a solid precipitate was formed. After 90 min excess aziridine was removed in an air stream at 20°, leaving an oily solid residue. This was dissolved in acetonitrile (10 ml) and the solution was absorbed on to silica gel (1.0 g), and remaining volatiles were removed by evaporation under reduced pressure at 20°. The solid obtained was added to the top of a column of silica gel (19.7 g, length 15 cm, diameter 2 cm) and the column eluted with acetonitrile. The elution of phenol was followed by TLC and after it was complete, subsequent eluate was collected and gave on evaporation to dryness under reduced pressure N-cyano-N'-methyl-1-aziridinoamidine (0.257 g, 77%), m.p. 130°-132.5°, Rf 0.64-0.66 (silica, acetonitrile).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739077
Source datasetuspto-grants-1988_04
ORD IDord-8ec1792ae5fc4df782364e7dc58301be
Source noteuspto-grants-1988_04