Réaction #4708

ord-c86fc35ded4042d5a2cef2319811c188

Équation de réaction

NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-hydrazine carbothioamide
CCCCN=C=O
n-butylisocyanate
→
CCCCNC(=O)NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
N-Butyl-2-[[3-[3-(1-piperidinylmethyl) phenoxy]propyl]aminothioxomethyl]-hydrazine carboxamide

Réactifs

NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-hydrazine carbothioamide
CCCCN=C=O
n-butylisocyanate

Réactifs

Aucun

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The compound is prepared by a method analogous to that of Example 9 from N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-hydrazine carbothioamide and n-butylisocyanate. The analytical values are summarized in Table I.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04727081uspto-grants-1988_02