4-iodo-1H-imidazole → (S)-5-(1H-imidazol-5-ylethynyl)-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]nicotinamide

HRID 607363Notes

Reaction equation

HRID 607363 reaction equation
[C:1]([C:3]1[CH:4]=[N:5][CH:6]=[C:7]([CH:20]=1)[C:8]([N:10]=[S@@:11]([CH3:19])(=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9])#[CH:2].I[C:22]1[NH:26][CH:25]=[N:24][CH:23]=1>>[NH:24]1[C:23]([C:2]#[C:1][C:3]2[CH:4]=[N:5][CH:6]=[C:7]([CH:20]=2)[C:8]([N:10]=[S@@:11]([CH3:19])(=[O:18])[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[O:9])=[CH:22][N:26]=[CH:25]1

Participants

3

Reactant 2

HCID 6065224-iodo-1H-imidazoleHCID 24953136(S)-5-ethynyl-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]nicotinamide

Product 1

HCID 24954181(S)-5-(1H-imidazol-5-ylethynyl)-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]nicotinamideYield 46%

Procedure

In a manner similar to that describe in Example 434, a mixture of (S)-5-ethynyl-N-[methyl(oxo)phenyl-λ6-sulfanylidene]nicotinamide and 5-iodo-1H-imidazole were reacted to give the title compound as a white foam (24 mg, 46%).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-b473a2c2736643e98389341b949ce4f9
Source dataset
uspto-grants-2011_03
Patent number
US07915443B2

Reaction notes

Loading…