Ammonia → HCID 131718020, compound

HRID 483523Notes

Reaction equation

HRID 483523 reaction equation
[NH:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH2:4][C:2]1=[O:3].[NH3:12].[CH3:13][OH:14]>>[C:13]([C:5]1([N:1]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH2:5][CH2:4][C:2]2=[O:3])[CH2:6][CH2:11][NH:1][CH2:2][CH2:4]1)(=[O:14])[NH2:12]

Participants

4

Procedure

1-{1-[4-(1-Ethoxy-1-iminomethyl)benzoyl]-4piperidinyl{-3,4-dihydrocarbostyril (1 g) is dissolved in methanol (10 ml) and thereto is added aqueous ammonia (10 ml) and the mixture is stirred at room temperature overnight. The solvent is concentrated and water is added to the residue. The mixture is extracted with chloroform, dried with sodium carbonate, concentrated and then purified by silica gel column chromatography (solvent: chloroform: methanol=10:1) and recrystallized from ethanol/n-hexane to give 1-[1-(4-carbamoyl-4-piperidinyl]-3,4-dihydrocarbostyril (0.2 g) as white powder, m.p.: 101°-104° C.

Workup

  1. concentrationThe solvent is concentrated
  2. additionwater is added to the residue
  3. extractionThe mixture is extracted with chloroform
  4. dry with materialdried with sodium carbonate
  5. concentrationconcentrated
  6. custompurified by silica gel column chromatography (solvent: chloroform: methanol=10:1)
  7. customrecrystallized from ethanol/n-hexane

Sources & evidence

ORD record
ord-104f3ffad3e14490a9cc33a30487a27d
Source dataset
uspto-grants-1993_07
Patent number
US05225402

Reaction notes

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