5-(Bromomethyl)pyrimidine → HCID 57383185, compound

HRID 536189Notes

Reaction equation

HRID 536189 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][O:17][C:18]3[CH:23]=[CH:22][NH:21][C:20](=[O:24])[N:19]=3)=[CH:11][CH:10]=2)=[CH:4][C:3]=1[C:25]([F:28])([F:27])[F:26].Br[CH2:30][C:31]1[CH:32]=[N:33][CH:34]=[N:35][CH:36]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:10]=[CH:11][C:12]([CH2:15][CH2:16][O:17][C:18]3[CH:23]=[CH:22][N:21]([CH2:30][C:31]4[CH:32]=[N:33][CH:34]=[N:35][CH:36]=4)[C:20](=[O:24])[N:19]=3)=[CH:13][CH:14]=2)=[CH:4][C:3]=1[C:25]([F:26])([F:28])[F:27]

Participants

3

Reactant 2

HCID 144349195-(Bromomethyl)pyrimidineHCID 178518454HCID 178518454, compound

Product 1

HCID 57383185HCID 57383185, compound

Procedure

The title compound was prepared by a procedure similar to that described for E1 starting from 4-{[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]oxy}-2(1H)-pyrimidinone and 5-(bromomethyl)pyrimidine. LC-MS (ESI): m/z 503 [M+H]+; 3.55 min (ret time).

Workup

  1. custom3.55 min (ret time)

Sources & evidence

ORD record
ord-6cdeaae703dd46e298f861517105d9d7
Source dataset
uspto-grants-2014_10
Patent number
US08859573B2

Reaction notes

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