Methyl 2-amino-2-methylpropanoate → HCID 71087695, compound

HRID 927332Notes

Reaction equation

HRID 927332 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:13]=[C:12]([C:14]([OH:16])=O)[CH:11]=[CH:10][CH:9]=1.[CH3:17][O:18][C:19](=[O:24])[C:20]([CH3:23])([CH3:22])[NH2:21]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:13]=[C:12]([C:14]([NH:21][C:20]([CH3:23])([CH3:22])[C:19]([O:18][CH3:17])=[O:24])=[O:16])[CH:11]=[CH:10][CH:9]=1

Participants

3

Reactant 2

HCID 4186341Methyl 2-amino-2-methylpropanoateHCID 247301346-(2-Chlorophenyl)pyridine-2-carboxylic acid

Product 1

HCID 71087695HCID 71087695, compound

Procedure

The title compound was synthesized in analogy to Example 1, using 6-(2-chlorophenyl)-2-pyridinecarboxylic acid (CAN 887982-21-0) and 2-methyl-alanine methyl ester as starting materials, MS (LC/MS): 333.1 (M+H).

Sources & evidence

ORD record
ord-ae0bc748ad6e4461a291a81b7e121d67
Source dataset
uspto-grants-2016_03
Patent number
US09290451B2

Reaction notes

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