Formaldehyde → Methyl 2-(5-(dimethylamino)pyridin-2-yl)acetate

HRID 572931Notes

Reaction equation

HRID 572931 reaction equation
N[C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[N:6][CH:7]=1.[CH2:13]=O.[BH3-][C:16]#[N:17].[Na+]>CO.CC(O)=O>[CH3:13][N:17]([CH3:16])[C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[N:6][CH:7]=1

Participants

6

Reactant 3

HCID 712FormaldehydeHCID 5003444Sodium cyanoborohydrideHCID 53659969Methyl 2-(5-aminopyridin-2-yl)acetate

Product 1

HCID 86719113Methyl 2-(5-(dimethylamino)pyridin-2-yl)acetate

Reagents, catalysts & solvents 2

HCID 176Acetic AcidCatalystHCID 887MethanolSolvent

Procedure

To the solution of methyl 2-(5-aminopyridin-2-yl)acetate (800 mg, 4.8 mmol) and paraformaldehyde (578.3 mg, 19.3 mmol) in methanol (20 mL) was added NaBH3CN (1.2 g, 19.26 mmol) and AcOH (1 drop, cat.). The mixture was stirred at room temperature for 12 h. Then, the reaction was quenched with aqueous ammonium chloride and extracted with DCM. The organic layer was with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by a standard method to get desired product.

Workup

  1. customThen, the reaction was quenched with aqueous ammonium chloride
  2. extractionextracted with DCM
  3. dry with materialdried over sodium sulfate
  4. customevaporated under reduced pressure
  5. customThe residue was purified by a standard method

Sources & evidence

ORD record
ord-d418b8ade1784f5387eee54b70baf3a3
Source dataset
uspto-grants-2015_05
Patent number
US09029531B2

Reaction notes

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