Reaction #78119

ord-d8bfd33ca5d444b7bd08fd151d4d726d

Reaction equation

Nc1cccnc1NCC1CCN(c2ccncc2)CC1
N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine
COc1ccc(C(=O)Cl)cc1
4-methoxybenzoyl chloride
COc1ccc(C(=O)Nc2cccnc2NCC2CCN(c3ccncc3)CC2)cc1
title compound
Yield 15.1%
COc1ccc(C(=O)Nc2cccnc2NCC2CCN(c3ccncc3)CC2)cc1
N3-(4-methoxybenzoyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine
Yield 15.1%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Using a similar procedure to that described in Example 2, Part D, N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine (300 mg, 1.06 mmol) and 4-methoxybenzoyl chloride (200 mg, 1.17 mmol) yielded 67 mg (15%) of the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06710057B2uspto-grants-2004_03