3-({3-[2-(4-Cyano-phenylamino)-acetylamino]-4-methylamino-benzoyl}-phenyl-amino)-propionic acid methyl ester → 3-({2-[(4-Cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-propionic acid methyl ester

HRID 68187Notes

Reaction equation

HRID 68187 reaction equation
[CH3:1][O:2][C:3](=[O:36])[CH2:4][CH2:5][N:6]([C:13](=[O:35])[C:14]1[CH:19]=[CH:18][C:17]([NH:20][CH3:21])=[C:16]([NH:22][C:23](=O)[CH2:24][NH:25][C:26]2[CH:31]=[CH:30][C:29]([C:32]#[N:33])=[CH:28][CH:27]=2)[CH:15]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(O)(=O)C>[CH3:1][O:2][C:3](=[O:36])[CH2:4][CH2:5][N:6]([C:13]([C:14]1[CH:19]=[CH:18][C:17]2[N:20]([CH3:21])[C:23]([CH2:24][NH:25][C:26]3[CH:27]=[CH:28][C:29]([C:32]#[N:33])=[CH:30][CH:31]=3)=[N:22][C:16]=2[CH:15]=1)=[O:35])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

3

Procedure

A solution of the product of 1c (22.6 mmol) in 100 mL concentrated acetic acid was heated to reflux for one hour. The solution was then evaporated to dryness, the remaining solid triturated with water and under stirring the pH was adjusted to about 8-9. The crude product was isolated through extraction with ethyl acetate and purified by chromatography on silica gel (eluent: dichloromethane/ethanol 1:1).

Workup

  1. temperatureto reflux for one hour
  2. customThe solution was then evaporated to dryness
  3. customthe remaining solid triturated with water

Sources & evidence

ORD record
ord-02d1c0d12ff84eb0839986a2614f494e
Source dataset
uspto-grants-2014_09
Patent number
US08821871B2

Reaction notes

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