2-Amino-5-methylpyridine → HCID 57504582, compound

HRID 1098096Notes

Reaction equation

HRID 1098096 reaction equation
[Br:1][CH:2]([CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH3:12])[C:3]([OH:5])=O.[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][N:15]=1>>[Br:1][CH:2]([CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH3:12])[C:3]([NH:13][C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][N:15]=1)=[O:5]

Participants

3

Reactant 2

HCID 153482-Amino-5-methylpyridineHCID 57438631HCID 57438631, compound

Product 1

HCID 57504582HCID 57504582, compound

Procedure

The title compound was prepared in a manner similar to that described for Intermediate A16 (Step 5) starting from 2-bromo-4-(2-methoxyethoxy)butanoic acid and 2-amino-5-picoline.

Sources & evidence

ORD record
ord-d5fc69781b3d42eaac4e05e6261028da
Source dataset
uspto-grants-2012_03
Patent number
US08143263B2

Reaction notes

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