2-Amino-5-methylpyridine → HCID 57504593, compound

HRID 1098108Notes

Reaction equation

HRID 1098108 reaction equation
[Si:1]([O:8][C@@H:9]([CH2:13][O:14][CH:15]([CH3:17])[CH3:16])[C:10]([OH:12])=O)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH3:18][C:19]1[CH:20]=[CH:21][C:22]([NH2:25])=[N:23][CH:24]=1>>[Si:1]([O:8][C@@H:9]([CH2:13][O:14][CH:15]([CH3:17])[CH3:16])[C:10]([NH:25][C:22]1[CH:21]=[CH:20][C:19]([CH3:18])=[CH:24][N:23]=1)=[O:12])([C:4]([CH3:5])([CH3:6])[CH3:7])([CH3:2])[CH3:3]

Participants

3

Reactant 2

HCID 153482-Amino-5-methylpyridineHCID 57504592HCID 57504592, compound

Product 1

HCID 57504593HCID 57504593, compound

Procedure

C7d was prepared in an analogous fashion to C4d from (S)-2-(tert-butyldimethylsilyloxy)-3-isopropoxypropanoic acid C7c and 5-methylpyridin-2-amine.

Sources & evidence

ORD record
ord-95a769ba0b544d68863bf5021ed615f5
Source dataset
uspto-grants-2012_03
Patent number
US08143263B2

Reaction notes

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