Toluene → HCID 19030882, compound

HRID 266801Notes

Reaction equation

HRID 266801 reaction equation
FC(F)(F)C(O)=O.[OH:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:37]=[CH:36][C:16]([C:17]([N:19]2[CH2:24][CH2:23][CH:22]([N:25]3[C:35]4[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH2:29][CH2:28][C:26]3=[O:27])[CH2:21][CH2:20]2)=[O:18])=[CH:15][CH:14]=1.[O:38]([C:40]#[N:41])[Na].C1(C)C=CC=CC=1>C(OCC)(=O)C.C(Cl)(Cl)Cl>[C:40]([O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([C:17]([N:19]2[CH2:20][CH2:21][CH:22]([N:25]3[C:35]4[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH2:29][CH2:28][C:26]3=[O:27])[CH2:23][CH2:24]2)=[O:18])=[CH:36][CH:37]=1)(=[O:38])[NH2:41]

Participants

7

Procedure

Trifluoroacetic acid (0.21 ml) is added dropwise with stirring to a mixture of 1-{1-[4-(3-hydroxypropoxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (0.51 g), NaOCN (0.16 g), toluene (5 ml) and chloroform (5 ml) at room temperature. After adding, the mixture is stirred at room temperature overnight. Ethyl acetate is added to the reaction mixture and the mixture is washed with saturated aqueous sodium hydrogen carbonate solution, water and saline solution successively and then dried with sodium sulfate. The solvent is distilled off and the resulting residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=100:1) to give 1-{1-[4-(3-carbamoyloxypropoxy)benzoyl-4-piperidinyl}-3,4-dihydrocarbostyril (0.15 g).

Workup

  1. additionAfter adding
  2. washthe mixture is washed with saturated aqueous sodium hydrogen carbonate solution, water and saline solution successively
  3. dry with materialdried with sodium sulfate
  4. distillationThe solvent is distilled off
  5. customthe resulting residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=100:1)

Sources & evidence

ORD record
ord-045eeadba2a24ab28847b3d7a8bb2502
Source dataset
uspto-grants-1997_07
Patent number
US05652247

Reaction notes

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