1,2-Dichloroethane → HCID 178469043, compound

HRID 1169902Notes

Reaction equation

HRID 1169902 reaction equation
[F:1][C:2]1[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[C:3]=1[C:4]([NH:6][C:7]1[C:8]([C:12]([OH:14])=O)=[N:9][NH:10][CH:11]=1)=[O:5].C(Cl)CCl.[CH:24]1[CH:25]=[CH:26][C:27]2[N:32](O)N=N[C:28]=2[CH:29]=1.[CH3:34][CH2:35][O:36][C:37](C)=[O:38]>CN(C=O)C>[CH2:35]([O:36][C:37]([CH:24]1[CH2:29][CH2:28][CH:27]([NH:32][C:12]([C:8]2[C:7]([NH:6][C:4](=[O:5])[C:3]3[C:15]([F:19])=[CH:16][CH:17]=[CH:18][C:2]=3[F:1])=[CH:11][NH:10][N:9]=2)=[O:14])[CH2:26][CH2:25]1)=[O:38])[CH3:34]

Participants

6

Reactant 4

HCID 111,2-DichloroethaneHCID 8857Ethyl AcetateHCID 757711-HydroxybenzotriazoleHCID 178524954HCID 178524954, compound

Product 1

HCID 178469043HCID 178469043, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A mixture of the ethyl ester (103 mg, 0.60 mmol), 4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid (134 mg, 0.50 mmol), EDC (115 mg, 0.60 mmol) and HOBt (81 mg, 0.60 mmol) in DMF (5 ml) was stirred at ambient temperature for 16 hours. The mixture was reduced in vacuo, the residue taken up in EtOAc and washed successively with saturated aqueous sodium bicarbonate, water and brine. The organic portion was dried (MgSO4) and reduced in vacuo to give 4-{[4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carbonyl]-amino}-cyclohexanecarboxylic acid ethyl ester (112 mg).

Workup

  1. washwashed successively with saturated aqueous sodium bicarbonate, water and brine
  2. dry with materialThe organic portion was dried (MgSO4)

Sources & evidence

ORD record
ord-6bfc3ceb7d794df4a181c317ea1bfd9e
Source dataset
uspto-grants-2010_11
Patent number
US07825140B2

Reaction notes

Loading…