Реакция #95386

ord-94e274c4bcfd482bbb4f48b3715bdd29

Уравнение реакции

O=C(CCl)Nc1nc2cc3nc(NC(=O)CCl)sc3cc2s1
2,6-bis-(chloroacetyl-amino)benzo[1,2-d:5,4-d']bisthiazole
CCC1CCCCN1
2-ethyl-piperidine
CCC1CCCCN1N(C(C)=O)c1nc2cc3nc(N(C(C)=O)N4CCCCC4CC)sc3cc2s1
compounds ( a )
Выход 47.0%
CCC1CCCCN1N(C(C)=O)c1nc2cc3nc(N(C(C)=O)N4CCCCC4CC)sc3cc2s1
2,6-Bis-(2-ethylpiperidino-acetylamino)-benzo[1,2-d:5,4-d']bisthiazole
Выход 47.0%
CCC1CCCCN1N(C(C)=O)c1nc2cc3nc(N)sc3cc2s1
( b )
Выход 37.0%
CCC1CCCCN1N(C(C)=O)c1nc2cc3nc(N)sc3cc2s1
2-Amino-6-(2-ethylpiperidino-acetylamino)-benzo[1,2-d:5,4-d']bisthiazole
Выход 37.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas refluxed for 2 hours

Методика

A mixture of 8.0 gm of 2,6-bis-(chloroacetyl-amino)benzo[1,2-d:5,4-d']bisthiazole, 10.0 gm of 2-ethyl-piperidine and 100 ml of dioxane was refluxed for 2 hours. The reaction mixture was worked up as described in Example 16; the compounds (a) (47% of theory, from ethanol), M.P. 201°-203° C., and (b) (37% of theory, from ethanol), M.P. 223°-225° C. were isolated.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04344946uspto-grants-1982_08