1-(Pyridin-4-yl)ethan-1-amine → (6,4'-Dimethoxy-biphenyl-3-ylmethyl)-(1-pyridin-4-yl-ethyl)-amine

HRID 1072244Notes

Reaction equation

HRID 1072244 reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)=[CH:7][C:6]([CH2:17][NH:18][CH:19](C2C=NC=CC=2)[CH3:20])=[CH:5][CH:4]=1.[N:27]1[CH:32]=[CH:31][C:30](C(N)C)=[CH:29][CH:28]=1.COC1C(C2C=CC(OC)=CC=2)=CC(C=O)=CC=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>>[CH3:1][O:2][C:3]1[C:8]([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)=[CH:7][C:6]([CH2:17][NH:18][CH:19]([C:30]2[CH:31]=[CH:32][N:27]=[CH:28][CH:29]=2)[CH3:20])=[CH:5][CH:4]=1

Participants

5

Procedure

The title compound was prepared by the same procedure for preparing (6,4′-dimethoxy-biphenyl-3-ylmethyl)-(1-pyridin-3-yl-ethyl)-amine from 1-Pyridin-4-yl-ethylamine (245 mg, 2 mmol), 6,4′-Dimethoxy-biphenyl-3-carbaldehyde (121 mg, 0.5 mmol) and sodium triacetoxyborohydride (212 mg, 1.0 mmol, Aldrich). The title compound was purified by column chromatography (silica gel, ethyl acetate) in form as white solid in 51% yield (89 mg, 0.26 mmol).

Workup

  1. customThe title compound was purified by column chromatography (silica gel, ethyl acetate) in form as white solid in 51% yield (89 mg, 0.26 mmol)

Sources & evidence

ORD record
ord-78a756b7f2824adab3c75c21df86a9d8
Source dataset
uspto-grants-2005_06
Patent number
US06908935B2

Reaction notes

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