Reaktion #50600

ord-6c21ad51386049a890bf9e863962f865

Reaktionsgleichung

COc1cc2oc(=O)ccc2cc1OCC1CO1
7-methoxy-6-(oxiranylmethoxy)-2H-1-benzopyran-2-one
OC1(c2ccccc2)CCNCC1
4-hydroxy-4-phenylpiperidine
Cl
Hydrochloride
COc1cc2oc(=O)ccc2cc1OCC(O)CN1CCC(O)(c2ccccc2)CC1
(±)-6-[2-hydroxy-3-(4-hydroxy-4-phenyl-1-piperidinyl)propoxy]-7-methoxy-2H-1-benzopyran-2-one
Ausbeute 69.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeMethod C (3 d at 40° C.)

Vorschrift

Method C (3 d at 40° C.); starting materials: 7-methoxy-6-(oxiranylmethoxy)-2H-1-benzopyran-2-one and 4-hydroxy-4-phenylpiperidine; yield 69%; fusion point 155°-157° C. (from isopropanol). Hydrochloride: method G; yield 88%; fusion point 202°-203° C. (from isopropanol).

Quelle

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