Reaction #433630

ord-b968ccedd0584457b42b4a3c19d603ac

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherwas prepared in analogy to Example 1 d

Procedure

The title compound was prepared in analogy to Example 1 d) from 7-(3-fluoro-benzyloxy)-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride [Example 1c)] and methoxy-acetic acid chloride with N-ethyl-diisopropylamine as the base. Yield: 98% of theory as a colourless oil; MS: m/e=344 (M+H)+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07173023B2uspto-grants-2007_02