HCID 9848330, compound → HCID 22626713, compound

HRID 277946Notes

Reaction equation

HRID 277946 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]([Br:29])=[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:24]=[CH:25][C:26]([Br:29])=[CH:27][CH:28]=1

Participants

3

Reactant 1

HCID 9848330HCID 9848330, compound

Product 1

HCID 22626713HCID 22626713, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The 2-trifluoroacetamido-3-(4-bromophenyl)-6-benzoyl-imidazo[1,2-a]pyridine (3.00 g, 6.15 mmol) was converted to product in a manner substantially analogous to Example 67 to yield 1.80 g. (75%). EA, MS(FD).

Workup

  1. customto yield 1.80 g

Sources & evidence

ORD record
ord-3c699aa17422433e9463bfb5a11cfc23
Source dataset
uspto-grants-2002_03
Patent number
US06358971B1

Reaction notes

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