2-Pyridinemethanamine → HCID 18399976, compound

HRID 912645Notes

Reaction equation

HRID 912645 reaction equation
[NH2:1][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1.C([N:17]=[C:18]=[S:19])(=O)C1C=CC=CC=1>C(Cl)Cl>[N:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[CH2:2][NH:1][C:18]([NH2:17])=[S:19]

Participants

4

Conditions

Temperature
0 °C

Procedure

2-(Aminomethyl)pyridine (2.0 g, 18.5 mmol) was added dropwise to a stirred solution of benzoyl isothiocyanate (3.3 g, 20.2 mmol) in CH2Cl2 (30 mL) at 0° C. The mixture was stirred at 0° C. for 4 h. The solvent was evaporated in vacuo and 1M sulfuric acid (40 mL) was added. The reaction mixture was stirred at rt for 19 h. The mixture was neutralized with saturated sodium carbonate (aq.). The oil that formed in the solution during neutralization was removed with a spatula. The solid was collected, washed and dried. The solid was then dissolved in sodium hydroxide (10% aq., 15 mL) and MeOH (5 mL) and the solution was stirred at r.t. for 20 h. The reaction mixture was neutralized with 2M sulfuric acid and the aqueous solution was extracted with ethyl acetate (2×50 mL). The organic phase was treated with activated charcoal, filtered, dried (Na2SO4) and evaporated. The residue was suspended in diethyl ether, filtered, washed with diethyl ether and dried, giving the title compound (1.35 g, 44%) as a solid. The crude product was used in the next step without further purification.

Workup

  1. customThe solvent was evaporated in vacuo and 1M sulfuric acid (40 mL)
  2. additionwas added
  3. stirringThe reaction mixture was stirred at rt for 19 h
  4. customThe oil that formed in the solution during neutralization
  5. customwas removed with a spatula
  6. customThe solid was collected
  7. washwashed
  8. customdried
  9. dissolutionThe solid was then dissolved in sodium hydroxide (10% aq., 15 mL)
  10. stirringMeOH (5 mL) and the solution was stirred at r.t. for 20 h
  11. extractionthe aqueous solution was extracted with ethyl acetate (2×50 mL)
  12. additionThe organic phase was treated with activated charcoal
  13. filtrationfiltered
  14. dry with materialdried (Na2SO4)
  15. customevaporated
  16. filtrationfiltered
  17. washwashed with diethyl ether
  18. customdried

Sources & evidence

ORD record
ord-7352bea0174f41659a4a172c86f54d19
Source dataset
uspto-grants-2011_09
Patent number
US08026244B2

Reaction notes

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