4-Methoxybenzylamine → HCID 118113913, compound

HRID 918831Notes

Reaction equation

HRID 918831 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][NH2:10])=[CH:5][CH:4]=1.[Br:11][C:12]1[CH:13]=[CH:14][C:15]2[N:16]([CH:18]=[C:19]([C:21](OCC)=[O:22])[N:20]=2)[CH:17]=1>>[Br:11][C:12]1[CH:13]=[CH:14][C:15]2[N:16]([CH:18]=[C:19]([C:21]([NH:10][CH2:9][C:6]3[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=3)=[O:22])[N:20]=2)[CH:17]=1

Participants

3

Reactant 2

HCID 754524-MethoxybenzylamineHCID 7141939Ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate

Product 1

HCID 118113913HCID 118113913, compound

Procedure

The title compound was prepared by essentially following the same procedures described for Intermediate I, using (4-methoxyphenyl)methanamine and ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate as starting materials.

Sources & evidence

ORD record
ord-befca6c76d7342d6a4de474c2e9a8cc7
Source dataset
uspto-grants-2016_03
Patent number
US09271969B2

Reaction notes

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