3-Pyridinecarboxaldehyde → 4-(3-Aminomethylpyridyl)-2-phenylbenzoylmethionine methyl ester

HRID 2121129Notes

Reaction equation

HRID 2121129 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]=O)[CH:2]=1.[CH3:9][O:10][C:11](=[O:33])[C@H:12]([CH2:29][CH2:30][S:31][CH3:32])[NH:13][C:14](=[O:28])[C:15]1[CH:20]=[CH:19][C:18](N)=[CH:17][C:16]=1[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.[BH3-]C#[N:36].[Na+].C([O-])(O)=O.[Na+]>CO.C(O)(=O)C>[CH3:9][O:10][C:11](=[O:33])[C@H:12]([CH2:29][CH2:30][S:31][CH3:32])[NH:13][C:14](=[O:28])[C:15]1[CH:20]=[CH:19][C:18]([C:2]2[C:3]([CH2:7][NH2:36])=[CH:4][CH:5]=[CH:6][N:1]=2)=[CH:17][C:16]=1[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

Participants

6

Procedure

A mixture of 3-pyridinecarboxaldehyde (1.0 equivalent), 4-amino-2-phenylbenzoyl methionine methyl ester (1.0 equivalent) and NaCNBH3 (1.0 equivalent) in methanol/acetic acid is stirred until the reaction is judged complete by TLC analysis. The mixture is poured into aqueous NaHCO3 and extracted into ethyl acetate which is dried and evaporated. Chromatography of the residue on silica gel affords the title compound.

Workup

  1. extractionextracted into ethyl acetate which
  2. customis dried
  3. customevaporated

Sources & evidence

ORD record
ord-d7491768a5624da38e37019ead68dc58
Source dataset
uspto-grants-2004_02
Patent number
US06693123B2

Reaction notes

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