2-Bromomethyl-5-(4-trifluoromethyl-phenyl)-pyrimidine → 3-{4-[5-(4-Trifluoromethyl-phenyl)-pyrimidin-2-ylmethoxy]-naphthalen-1-yl}-propionic acid ethyl ester

HRID 1726998Notes

Reaction equation

HRID 1726998 reaction equation
[CH2:1]([O:3][C:4](=[O:18])[CH2:5][CH2:6][C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([OH:17])=[CH:9][CH:8]=1)[CH3:2].Br[CH2:20][C:21]1[N:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:29][CH:28]=2)=[CH:23][N:22]=1>>[CH2:1]([O:3][C:4](=[O:18])[CH2:5][CH2:6][C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([O:17][CH2:20][C:21]2[N:22]=[CH:23][C:24]([C:27]3[CH:28]=[CH:29][C:30]([C:33]([F:36])([F:34])[F:35])=[CH:31][CH:32]=3)=[CH:25][N:26]=2)=[CH:9][CH:8]=1)[CH3:2]

Participants

3

Reactant 2

HCID 219359222-Bromomethyl-5-(4-trifluoromethyl-phenyl)-pyrimidineHCID 58566550Ethyl 3-(4-hydroxynaphthalen-1-yl)propanoate

Product 1

HCID 690373643-{4-[5-(4-Trifluoromethyl-phenyl)-pyrimidin-2-ylmethoxy]-naphthalen-1-yl}-propionic acid ethyl ester

Procedure

A] In analogy to the procedures described in example 5C] and 5D], 3-(4-hydroxy-naphthalen-1-yl)-propionic acid ethyl ester [Helvetica Chimica Acta (2001), 84(8), 2198-2211] was reacted with 2-bromomethyl-5-(4-trifluoromethyl-phenyl)-pyrimidine (example 11C]) to give 3-{4-[5-(4-trifluoromethyl-phenyl)-pyrimidin-2-ylmethoxy]-naphthalen-1-yl}-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as colorless solid.

Sources & evidence

ORD record
ord-d1af9ac3037e43ce98d24b95c0b83258
Source dataset
uspto-grants-2009_02
Patent number
US07495001B2

Reaction notes

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