Acetic Acid → HCID 58611965, compound

HRID 751263Notes

Reaction equation

HRID 751263 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([CH:11]=O)=[CH:9][N:10]=2)[CH:7]=1.[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1.C(O)(=O)C.[BH4-].[Na+]>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([CH2:11][N:13]3[CH2:18][CH2:17][O:16][CH2:15][CH2:14]3)=[CH:9][N:10]=2)[CH:7]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 8083MorpholineHCID 4311764Sodium borohydrideHCID 213456766-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde

Product 1

HCID 58611965HCID 58611965, compoundYield 42.4%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Reflux a solution of 6-bromo-imidazo[1,2-a]pyridine-3-carbaldehyde (J. Med. Chem. 1970, 13(6), 1048-51; 0.45 g, 1.99 mmol), morpholine (1.7 g, 19.9 mmol), and acetic acid (0.12 mL, 1.99 mmol) in toluene (200 mL) for 3 h. Concentrate to dryness and re-dissolve in methanol (100 mL). Add sodium borohydride (0.226 g, 5.99 mmol) in portions and stir for 30 min. Concentrate to ˜25 mL, dilute with saturated aqueous sodium bicarbonate, extract into ethyl acetate, combine and concentrate. Flash chromatography gives the titled compound (0.25 g, 42%). MS ES+ m/e 295.8, 297.8 (M+1). 1H NMR (400 MHz, DMSO-d6) δ 8.69 (s, 1H), 7.54 (d, J=10 Hz, 1H), 7.51 (s, 1H), 7.35 (d, J=10 Hz, 1H), 3.81 (s, 2H), 3.52 (t, J=4 Hz, 1H), 2.35 (t,J=4 Hz, 4H).

Workup

  1. concentrationConcentrate to dryness
  2. dissolutionre-dissolve in methanol (100 mL)
  3. concentrationConcentrate to ˜25 mL
  4. additiondilute with saturated aqueous sodium bicarbonate
  5. extractionextract into ethyl acetate
  6. concentrationconcentrate

Sources & evidence

ORD record
ord-6a8c762d11ac46e89239b29e669b2ca3
Source dataset
uspto-grants-2008_07
Patent number
US07405299B2

Reaction notes

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