HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Sodium hydride → 3-[4-(2-cyano-2-phenylethyl)phenyl]methyl-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine

HRID 2255572
Notes
Print preview

Reaction equation

HRID 2255572 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[N:8]=[C:9]([CH2:11][CH2:12][CH3:13])[NH:10][C:3]=12.[H-].[Na+].Br[CH2:17][C:18]1[CH:23]=[CH:22][C:21]([CH2:24][CH:25]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:26]#[N:27])=[CH:20][CH:19]=1>CN(C=O)C>[C:26]([CH:25]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[CH2:24][C:21]1[CH:22]=[CH:23][C:18]([CH2:17][N:8]2[C:4]3=[N:5][CH:6]=[CH:7][C:2]([CH3:1])=[C:3]3[N:10]=[C:9]2[CH2:11][CH2:12][CH3:13])=[CH:19][CH:20]=1)#[N:27]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 24758Sodium hydrideHCID 150208527-Methyl-2-propyl-1H-imidazo[4,5-b]pyridineHCID 193855943-[4-(Bromomethyl)phenyl]2-phenylpropanonitrile

Product 1

HCID 197381193-[4-(2-cyano-2-phenylethyl)phenyl]methyl-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridineYield 19.1%

Reagents, catalysts & solvents 1

HCID 6228
Dimethylformamide
Solvent
2×

Procedure

To a solution of 7-methyl-2-propylimidazo [4,5-b]pyridine (106 mg, 0.61 mmol) in DMF (3 mL) was added NaH (0.91 mmol). The suspension was stirred at room temperature for 30 minutes, at which time a solution of the product of Step D (200 mg, 0.667 mmol) in DMF (2 mL) was added. The mixture was stirred for 2 hours at room temperature, quenched with water, and then concentrated in vacuo. The residue was partitioned between water and EtOAc, and the combined organic layers were washed with brine, dried (K2CO3), filtered, and evaporated in vacuo. The residue was chromatographed on a silica gel flash chromatography column eluted with 50% ethyl acetate/hexane to afford 46 mg (19%) of the title compound.

Workup

  1. additionwas added
  2. customquenched with water
  3. concentrationconcentrated in vacuo
  4. customThe residue was partitioned between water and EtOAc
  5. washthe combined organic layers were washed with brine
  6. dry with materialdried (K2CO3)
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. customThe residue was chromatographed on a silica gel flash chromatography column
  10. washeluted with 50% ethyl acetate/hexane

Sources & evidence

ORD record
ord-acaff30b281d49a4b8e62b363b4d0008
Source dataset
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05240938

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes