HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-cyano-O-phenyl-N'-[3-(3-(piperidinomethyl)phenoxy]propyl]isourea → HCID 54452316, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-cyano-O-phenyl-N'-[3-(3-(piperidinomethyl)phenoxy]propyl]isourea | HCID 13486636 | — |
| Reactant | N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,4-butanediamine | HCID 19762574 | — |
| Product | HCID 54452316 | HCID 54452316 | — |
Reaction Steps
Preparation is effected analogously to Example 1, using 0.33 g (1.0 mmol) of N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,4-butanediamine and the equimolar amount of N-cyano-O-phenyl-N'-[3-[3-(piperidinomethyl)phenoxy]propyl]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. [%])=629 ([M+H]+, 5), 229 (84), 109 (100); IR (KBr): 2166 cm-1 (C≡N). For further analysis, a portion of the compound is converted into the tartaric acid salt and recrystallised from ethanol/acetonitrile/isopropanol; m.p. 84°-86° C. (ethanol/acetonitrile/isopropanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212187 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-ccbb71e802d045de8e4d3a16077a682e |
| Source note | uspto-grants-1993_05 |