Potassium Carbonate → HCID 59446528, compound

HRID 1510314Notes

Reaction equation

HRID 1510314 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([OH:13])=O)=[CH:5]2.[Cl:14][C:15]1[CH:16]=[C:17]([S:22]([N:25]([CH2:35][P:36](=[O:43])([O:40][CH2:41][CH3:42])[O:37][CH2:38][CH3:39])[C:26]2[CH:27]=[C:28]3[C:32](=[CH:33][CH:34]=2)[NH:31][CH2:30][CH2:29]3)(=[O:24])=[O:23])[CH:18]=[C:19]([Cl:21])[CH:20]=1.C(=O)([O-])[O-].[K+].[K+]>S(Cl)(Cl)=O.ClCCl.CN(C)C=O.C(OCC)(=O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([N:31]1[C:32]3[C:28](=[CH:27][C:26]([N:25]([CH2:35][P:36](=[O:43])([O:37][CH2:38][CH3:39])[O:40][CH2:41][CH3:42])[S:22]([C:17]4[CH:16]=[C:15]([Cl:14])[CH:20]=[C:19]([Cl:21])[CH:18]=4)(=[O:24])=[O:23])=[CH:34][CH:33]=3)[CH2:29][CH2:30]1)=[O:13])=[CH:5]2

Participants

8

Conditions

Temperature
80 °C

Procedure

50 mg 5-chloro-1H-indole-2-carboxylic acid are dissolved in 2 ml of thionyl chloride and heated to 80° C. for 1 hour. The solvent is eliminated in vacuo and the residue is twice combined with dichloromethane and this is again eliminated in vacuo. The residue is taken up in 5 ml dichloromethane and the solution is added dropwise to a mixture of 100 mg diethyl {[(3,5-dichloro-phenylsulphonyl)-(2,3-dihydro-1H-indol-5-yl)-amino]-methyl}-phosphonate and 60 mg potassium carbonate in 2 ml dimethylformamide. The mixture is stirred for 2 hours at ambient temperature, diluted with ethyl acetate and washed with 1 N HCl and saturated sodium chloride solution. After drying with magnesium sulphate the solvents are eliminated in vacuo and the residue is chromatographed on silica gel (dichloromethane/methanol 95:5 to 70:30).

Workup

  1. washwashed with 1 N HCl and saturated sodium chloride solution
  2. dry with materialAfter drying with magnesium sulphate the solvents
  3. customthe residue is chromatographed on silica gel (dichloromethane/methanol 95:5 to 70:30)

Sources & evidence

ORD record
ord-582cb1886d2b481bab0aa7ec7a88e9f3
Source dataset
uspto-grants-2012_07
Patent number
US08211923B2

Reaction notes

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