Reacción #565233

ord-fd138a62c7684a99a2cd684fab6d1b45

Ecuación de reacción

ClCc1ccc2ccccc2n1
2-chloromethyl quinoline
N=C(N)NN.O=C(O)O
amino guanidine bicarbonate
CC(=NNC(=N)N)c1cccc(OCc2ccc3ccccc3n2)c1
product
Rendimiento 65.0%
CC(=NNC(=N)N)c1cccc(OCc2ccc3ccccc3n2)c1
2-[1-[3-(2-Quinolinylmethoxy)phenyl]ethylidene]hydrazinecarboximidamide
Rendimiento 65.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrois prepared (13.1 g, m.p. 57°-59° C., 47% yield)

Procedimiento

In a similar manner to Example 1A and using 2-chloromethyl quinoline, 3-(2-quinolinylmethoxy)acetophenone is prepared (13.1 g, m.p. 57°-59° C., 47% yield). This product is reacted with amino guanidine bicarbonate as in 1B above to give 2.35 g of product (65% yield), m.p. 168°-170° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04889935uspto-grants-1989_12