Réaction #4704

ord-81260fd740e24913832b9d137938d376

Équation de réaction

NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl] hydrazine carbothioamide
O=C(N=C=S)c1ccccc1
benzoyl isothiocyanate
→
O=C(NC(=S)NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1)c1ccccc1
N-Benzoyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]1,2-hydrazine dicarbothioamide

Réactifs

NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl] hydrazine carbothioamide
O=C(N=C=S)c1ccccc1
benzoyl isothiocyanate

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 5 from N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl] hydrazine carbothioamide and benzoyl isothiocyanate. The analytical values are summarized in Table I.

Source

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