HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19762513, compound → HCID 178484313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19762513 | HCID 19762513 | — |
| Reactant | HCID 178512334 | HCID 178512334 | — |
| Product | HCID 178484313 | HCID 178484313 | — |
Reaction Steps
Preparation is effected analogously to Example 1, using 0.30 g (1.0 mmol) of N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,2-ethanediamine and the equimolar amount of N-cyano-N'-[2-[[(2-guanidino-4-thiazolyl)methyl]thio]ethyl]-O-phenyl-isourea as starting materials. Working up by chromatography analogously to Example 1 yields the purified title compound in the form of a viscous oil; MS (+FAB method): m/z (rel. int. [%])=584 ([M+H]+, 3), 109 (100); IR (KBr): 2165 cm-1 (C≡N). For further analysis, a portion of the compound is converted into the tartaric acid salt and recrystalised from isopropanol/ether; m.p.: 109° C. (isopropanol/ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212187 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-65be5a1bf38442ada3a1653d041b8d56 |
| Source note | uspto-grants-1993_05 |