Reacción #2072153

ord-35d5a795317c42498a15108fbb9a0f54

Ecuación de reacción

O=C(Cl)c1ccc2cc(Br)ccc2c1
6-Bromo-naphthalene-2-carbonyl chloride
Nc1ccc2c(c1)NCC(CO)C2
(7-amino-1,2,3,4-tetrahydro-quinolin-3-yl)-methanol
O=C(Nc1ccc2c(c1)NCC(CO)C2)c1ccc2cc(Br)ccc2c1
title compound
O=C(Nc1ccc2c(c1)NCC(CO)C2)c1ccc2cc(Br)ccc2c1
6-Bromo-naphthalene-2-carboxylic acid (3-hydroxymethyl-1,2,3,4-tetrahydro-quinolin-7-yl)-amide

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThis material was prepared analogous to the procedure
  2. 2
    Otroprepared

Procedimiento

This material was prepared analogous to the procedure described for Example 1(c). 6-Bromo-naphthalene-2-carbonyl chloride, Example 2(a), (258 mg, 0.96 mmol) reacted with (7-amino-1,2,3,4-tetrahydro-quinolin-3-yl)-methanol (171 mg, 0.96 mmol, prepared according to the procedure described in WO03049702) to give the title compound as an light-brown amorphous solid. MS (ESI, pos. ion) m/z: 413 (M+1).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07544803B2uspto-grants-2009_06