2-Amino-5-bromopyridine → HCID 11245021, compound

HRID 558384Notes

Reaction equation

HRID 558384 reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]([OH:11])=O)=[CH:7][C:6]([C:12]([NH2:14])=[O:13])=[CH:5][CH:4]=1.[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][N:17]=1>>[Br:22][C:19]1[CH:20]=[CH:21][C:16]([NH:15][C:9](=[O:11])[C:8]2[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=2[O:2][CH3:1])[C:12]([NH2:14])=[O:13])=[N:17][CH:18]=1

Participants

3

Reactant 2

HCID 706222-Amino-5-bromopyridineHCID 132228085-Carbamoyl-2-methoxybenzoic acid

Product 1

HCID 11245021HCID 11245021, compound

Procedure

The captioned compound was synthesized from 6-methoxyisophthalamic acid and 2-amino-5-bromopyridine by the same procedure as in the manufacturing method described in step C of Example 1-3-1.

Sources & evidence

ORD record
ord-3756420a5afa4c16965d0b81810ec832
Source dataset
uspto-grants-2011_11
Patent number
US08063046B2

Reaction notes

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