Picolinic acid → HCID 21221047, compound

HRID 1584896Notes

Reaction equation

HRID 1584896 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([OH:9])=O.C(=[N:17][CH2:18][CH:19]1[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]1)C1C=CC=CC=1.S([O-])(O)(=O)=O.[K+]>ClCCl>[NH2:17][CH2:18][CH:19]1[CH2:24][CH2:23][N:22]([C:7]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)=[O:9])[CH2:21][CH2:20]1

Participants

5

Procedure

N,N'-Carbonyl diimidazole (6.58 g) was added to a suspension of pyridine-2-carboxylic acid (5.0 g) in dichloromethane (75 ml) stirring under nitrogen at ambient temperature. Stirring continued until gas evolution had ceased (~2 hours) then N-benzylidene-1-(4-piperidyl)methylamine (8.2 g) was added and the reaction mixture stirred for 18 hours. The solvent was evaporated to give a viscous yellow oil, which was then stirred with aqueous potassium hydrogen sulphate solution (1 M; 200 ml) for 18 hours. The mixture was washed with dichloromethane (2×250 ml) and adjusted to pH 14 with aqueous sodium hydroxide solution (5 M) then extracted with methane (3×250 ml). The combined extracts were dried over magnesium and the the solvent removed in vacuo to give 4-(aminomethyl)-1-(2-pyridylcarbonyl)piperidine (5.2 g) as a viscous yellow oil.

Workup

  1. stirringStirring
  2. custom(~2 hours)
  3. stirringthe reaction mixture stirred for 18 hours
  4. customThe solvent was evaporated
  5. customto give a viscous yellow oil, which
  6. washThe mixture was washed with dichloromethane (2×250 ml)
  7. extractionthen extracted with methane (3×250 ml)
  8. dry with materialThe combined extracts were dried over magnesium
  9. customthe the solvent removed in vacuo

Sources & evidence

ORD record
ord-c5bfdf09b0184ad39182f26a08672ebf
Source dataset
uspto-grants-1999_08
Patent number
US05935973

Reaction notes

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