تفاعل #43647

ord-2ed63c1b192a4d2ead674ec3f2add09b

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas prepared) in 71% yield

الإجراء التجريبي

The title compound was prepared from (4R)-4-[(4-amino-1-piperidinyl)methyl]-3-fluoro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one Enantiomer 1 and 2,3-dihydro-1,4-benzodioxin-6-carboxaldehyde (Aldrich) according to the general method of Example 2(h) (except that the dihydrochloride was prepared) in 71% yield.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07732461B2uspto-grants-2010_06