Reaktion #50632

ord-29ae1e67f57a4e9cbf6cce38fbf412f8

Reaktionsgleichung

O=C([O-])/C=C/C(=O)[O-]
Fumarate
O=C([O-])O.[K+]
potassium hydrogencarbonate
COc1cc2oc(=O)c3c(c2cc1OCCCCl)CCC3
8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
Cl.Cl.c1cnc(N2CCNCC2)nc1
1-(2-pyrimidinyl)piperazine dihydrochloride
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCN(c2ncccn2)CC1)CCC3
2,3-dihydro-7-methoxy-8-{3-[4-(2-pyrimidinyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-one
Ausbeute 54.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Method B (60 h at 50° C.; 4 equivalents of potassium hydrogencarbonate); starting materials: 8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 83) and 1-(2-pyrimidinyl)piperazine dihydrochloride; yield 54%; fusion point 184°-186° C. (from chloroform and ethanol). Fumarate: method E; yield 77%; fusion point 226°-228° C. (from acetone).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05428038uspto-grants-1995_06