Acetic Acid → (4-((Pyridin-2-ylamino)methyl)phenyl)methanol

HRID 7185

Reaction equation

HRID 7185 reaction equation
O[CH2:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[CH:5][CH:4]=1.[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C1COCC1>[N:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[NH:11][CH2:2][C:3]1[CH:10]=[CH:9][C:6]([CH2:7][OH:8])=[CH:5][CH:4]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 104392-AminopyridineHCID 5563304-(Hydroxymethyl)benzaldehydeHCID 5049666Sodium triacetoxyborohydride

Product 1

HCID 22018543(4-((Pyridin-2-ylamino)methyl)phenyl)methanolYield 74%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Using general procedure B: Reaction of 4-hydroxymethyl-benzaldehyde (1.01 g, 7.42 mmol), 2-aminopyridine (697 mg, 7.42 mmol), acetic acid (0.5 mL) and sodium triacetoxyborohydride (3.2 g, 14.8 mmol) in THF (20 mL) at room temperature under N2 for 40 min., then one hour at 50° C., followed by purification of crude material using chromatography on silica gel (2:2:96 CH3OH—NH3 H2O—CH2Cl2), afforded the title compound (1.17 g, 74%) as white foam.

Workup

  1. customone hour at 50° C., followed by purification of crude material

Sources & evidence

ORD record
ord-5a2f7a20ec2f494cadf3ca0313a915ff
Source dataset
uspto-grants-2006_08
Patent number
US07084155B2

Linked notes

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