1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4'-(2,6-Difluoro-benzoylamino)-6-methyl-biphenyl-3-carboxylic acid (2,2-diethoxy-ethyl)-amide

HRID 2047500Notes

Reaction equation

HRID 2047500 reaction equation
[F:1][C:2]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]2[C:18]([CH3:19])=[CH:17][CH:16]=[C:15]([C:20](O)=[O:21])[CH:14]=2)=[CH:9][CH:8]=1)=[O:5].[CH2:28]([O:30][CH:31]([O:34][CH2:35][CH3:36])[CH2:32][NH2:33])[CH3:29].CN(C)CCCN=C=NCC>CN(C=O)C.O>[CH2:28]([O:30][CH:31]([O:34][CH2:35][CH3:36])[CH2:32][NH:33][C:20]([C:15]1[CH:14]=[C:13]([C:10]2[CH:11]=[CH:12][C:7]([NH:6][C:4](=[O:5])[C:3]3[C:2]([F:1])=[CH:26][CH:25]=[CH:24][C:23]=3[F:27])=[CH:8][CH:9]=2)[C:18]([CH3:19])=[CH:17][CH:16]=1)=[O:21])[CH3:29]

Participants

6

Procedure

Compound 1 was hydrolyzed by heating it in a solution of LiOH to yield 4′-(2,6-difluoro-benzoylamino)-6-methyl-biphenyl-3-carboxylic acid. A mixture of 4′-(2,6-difluoro-benzoylamino)-6-methyl-biphenyl-3-carboxylic acid (800 mg, 2.2 mmol), 2,2-diethoxy-ethylamine (0.32 mL, 2.2. mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) (5 mmol) in dry DMF (5 mL) was stirred at room temperature for 24 h. The mixture was diluted with water (20 mL) and extracted with ethyl acetate (EtOAc) (2×20 mL). The organic extract was washed with water and dried. The oil obtained on concentration of the organic layer was purified by flash chromatograghed on silica gel to give 4′-(2,6-difluoro-benzoylamino)-6-methyl-biphenyl-3-carboxylic acid (2,2-diethoxy-ethyl)-amide as colorless oil (0.68 g).

Workup

  1. extractionextracted with ethyl acetate (EtOAc) (2×20 mL)
  2. extractionThe organic extract
  3. washwas washed with water
  4. customdried
  5. customThe oil obtained on concentration of the organic layer
  6. customwas purified by flash

Sources & evidence

ORD record
ord-172b334c6a904f11baf72c9f623e6c76
Source dataset
uspto-grants-2013_11
Patent number
US08592486B2

Reaction notes

Loading…