HCID 22626698, compound → HCID 22626755, compound

HRID 277944Notes

Reaction equation

HRID 277944 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[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=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[CH2:23][C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1

Participants

3

Reactant 1

HCID 22626698HCID 22626698, compound

Product 1

HCID 22626755HCID 22626755, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The 2-trifluoroacetamido-3-benzyl-6-benzoyl-imidazo[1,2-a]pyridine (2.14 g, 5.06 mmol) was converted to product in a manner substantially analogous to Example 56 to yield 1.29 g. (78.2%). EA, MS(FD).

Workup

  1. customto yield 1.29 g

Sources & evidence

ORD record
ord-5bbaaba8a4fd41cd947252eeceea7b19
Source dataset
uspto-grants-2002_03
Patent number
US06358971B1

Reaction notes

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