Reacción #62929

ord-11a2341c46d34299aa5811b7d2fe3d60

Ecuación de reacción

Cl.Cl.Nc1c(F)c(N)c(F)c(F)c1F
dihydrochloride
CCCN1CCC=C2c3nc(NC(=O)C(C)C)sc3CCC21
(±) N-(4,5,5a,6,7,8-hexahydro-6-propylthiazolo[4,5-f]quinolin-2-yl)-2-methylpropanamide
CN1CCC=C2c3nc(N)sc3CCC21
title compound
CN1CCC=C2c3nc(N)sc3CCC21
(+) 4,5,5a,6,7,8-Hexahydro-6-methylthiazolo[4,5-f]quinolin-2-amine

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

In a process analogous to Example 16 by substituting (±) N-(4,5,5a,6,7,8-hexahydro-6-methylthiazolo[4,5-f]quinolin-2-yl)-2-methylpropanamide (Example 15) for (±) N-(4,5,5a,6,7,8-hexahydro-6-propylthiazolo[4,5-f]quinolin-2-yl)-2-methylpropanamide (Example 15c), the title compound can be prepared as its dihydrochloride salt, hydrate; mp 265°-267° C. (dec.). [α]D =+164.4° (C=1.17, H2O).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04762843uspto-grants-1988_08