Sodium hydride → 7-((4-((2-chloropyridin-4-yl)oxy)-3-fluorobenzyl)oxy)-1-methyl-2,3-dihydroimidaz-o[1,2-c]pyrimidin-5(1H)-one

HRID 873218Notes

Reaction equation

HRID 873218 reaction equation
Cl[C:2]1[CH:3]=[C:4]2[N:11]([CH3:12])[CH2:10][CH2:9][N:5]2[C:6](=[O:8])[N:7]=1.[H-].[Na+].[Cl:15][C:16]1[CH:21]=[C:20]([O:22][C:23]2[CH:28]=[CH:27][C:26]([CH2:29][OH:30])=[CH:25][C:24]=2[F:31])[CH:19]=[CH:18][N:17]=1>CN(C=O)C>[Cl:15][C:16]1[CH:21]=[C:20]([O:22][C:23]2[CH:28]=[CH:27][C:26]([CH2:29][O:30][C:2]3[CH:3]=[C:4]4[N:11]([CH3:12])[CH2:10][CH2:9][N:5]4[C:6](=[O:8])[N:7]=3)=[CH:25][C:24]=2[F:31])[CH:19]=[CH:18][N:17]=1

Participants

5

Procedure

Prepared in a manner similar to that described for E1 using 7-chloro-1-methyl-2,3-dihydroimidazo[1,2-c]pyrimidin-5(1H)-one (50 mg, 0.269 mmol), sodium hydride (21.55 mg, 0.539 mmol) and (4-((2-chloropyridin-4-yl)oxy)-3-fluorophenyl)methanol (68.3 mg, 0.269 mmol) in DMF (2 mL).

Workup

  1. customPrepared in a manner similar to

Sources & evidence

ORD record
ord-d2200cf849404e25a483e642980827fe
Source dataset
uspto-grants-2015_03
Patent number
US08975400B2

Reaction notes

Loading…