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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aziridine | HCID 9033 | — |
| Reactant | HCID 13186920 | HCID 13186920 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-cyano-N'-methyl-1-aziridinoamidine | HCID 13150956 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04739077 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-8ec1792ae5fc4df782364e7dc58301be |
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| Source note | uspto-grants-1988_04 |
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