Stannous chloride dihydrate → HCID 15907986, compound

HRID 2230881Notes

Reaction equation

HRID 2230881 reaction equation
O.O.[Sn](Cl)Cl.[N:6]([CH:9]([C:11]1[CH:16]=[CH:15][C:14]([NH:17][C:18](=[S:34])[NH:19][C:20]2[CH:25]=[CH:24][C:23]([NH:26][C:27]([C:29]3[O:30][CH:31]=[CH:32][CH:33]=3)=[O:28])=[CH:22][CH:21]=2)=[CH:13][C:12]=1[Cl:35])[CH3:10])=[N+]=[N-]>CO.C(OCC)(=O)C>[NH2:6][CH:9]([C:11]1[CH:16]=[CH:15][C:14]([NH:17][C:18](=[S:34])[NH:19][C:20]2[CH:21]=[CH:22][C:23]([NH:26][C:27]([C:29]3[O:30][CH:31]=[CH:32][CH:33]=3)=[O:28])=[CH:24][CH:25]=2)=[CH:13][C:12]=1[Cl:35])[CH3:10]

Participants

5

Procedure

To a solution of tin(II) chloride dihydrate (0.25 g) in methanol (2.5 mL) is added furan-2-carboxylic acid (4-{3-[4-(1-azido-ethyl)-3-chloro-phenyl]-thioureido}-phenyl)-amide (0.22 g) and the solution is stirred for approximately 15 hours at room temperature. The solution is then diluted with ethyl acetate, washed successively with saturated aqueous sodium bicarbonate then saturated aqueous sodium chloride, then dried over anhydrous sodium sulfate. After removal of the solvent by evaporation under reduced pressure the residue is chromatographed over silica gel (8% methanol in dichloromethane containing 1% triethylamine is used as the eluant) to provide the desired product as a yellow solid.

Workup

  1. washwashed successively with saturated aqueous sodium bicarbonate
  2. dry with materialsaturated aqueous sodium chloride, then dried over anhydrous sodium sulfate
  3. customAfter removal of the solvent
  4. customby evaporation under reduced pressure the residue
  5. customis chromatographed over silica gel (8% methanol in dichloromethane containing 1% triethylamine

Sources & evidence

ORD record
ord-9ec10219512344508f30d69539af3297
Source dataset
uspto-grants-2002_07
Patent number
US06426355B1

Reaction notes

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