HCID 22626707, compound → HCID 22626729, compound

HRID 277961Notes

Reaction equation

HRID 277961 reaction equation
FC(F)(F)C([NH:5][C:6]1[N:7]=[C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:21])[C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:10][N:9]2[C:22]=1[C:23]1[CH:28]=[CH:27][C:26]([N+:29]([O-:31])=[O:30])=[CH:25][CH:24]=1)=O>CC(=O)OCC>[NH2:5][C:6]1[N:7]=[C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:21])[C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)=[CH:10][N:9]2[C:22]=1[C:23]1[CH:28]=[CH:27][C:26]([N+:29]([O-:31])=[O:30])=[CH:25][CH:24]=1

Participants

3

Reactant 1

HCID 22626707HCID 22626707, compound

Product 1

HCID 22626729HCID 22626729, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The 2-trifluoroacetamido-3-(4-nitrophenyl)-6-benzoyl-imidazo[1,2-a]pyridine (8.59 g, 18.9 mmol) was converted to product in a manner substantially analogous to Example 67 to yield 5.04 g. (74.4%). EA, MS(FD).

Workup

  1. customto yield 5.04 g

Sources & evidence

ORD record
ord-7bb679a1a84f444cafb353339c7e3d11
Source dataset
uspto-grants-2002_03
Patent number
US06358971B1

Reaction notes

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