Acetic Acid → Sodium Bicarbonate

HRID 1836682Notes

Reaction equation

HRID 1836682 reaction equation
[Br:1][C:2]1[C:7]([CH:8]=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[C:10]1([N:16]2[C:20]3([CH2:25][CH2:24][NH:23][CH2:22][CH2:21]3)[C:19](=[O:26])[NH:18][CH2:17]2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[C:27]([OH:30])(=[O:29])C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+:44]>C1COCC1.O>[C:27](=[O:29])([OH:9])[O-:30].[Na+:44].[Br:1][C:2]1[C:7]([CH2:8][N:23]2[CH2:22][CH2:21][C:20]3([N:16]([C:10]4[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=4)[CH2:17][NH:18][C:19]3=[O:26])[CH2:25][CH2:24]2)=[CH:6][CH:5]=[CH:4][N:3]=1

Participants

8

Procedure

To a stirring solution of 2-bromo-pyridine-3-carbaldehyde(0.68 g, 3.6 mmol) were added 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (0.846 g, 3.6 mmol), and acetic acid(1.1 g, 18 mmol) in THF (40.0 ml) and sodium triacetoxyborohydride (1.55 g, 7.3 mmol) and the resulting reaction mixture stirred at room temperature overnight. Water (50 ml) was added and the reaction mixture solution was extracted with ethyl acetate three times. The combined organic layers were dried over MgSO4. The solvent was removed and the resulting residue was purified over silica gel column eluted with methylene chloride (97%), methanol(2%), acetic acid(1%) and then with saturated sodium bicarbonate solution to yield 8-(2-bromo-pyridin-3-ylmethyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one as a white solid.

Workup

  1. customthe resulting reaction mixture
  2. extractionthe reaction mixture solution was extracted with ethyl acetate three times
  3. dry with materialThe combined organic layers were dried over MgSO4
  4. customThe solvent was removed
  5. customthe resulting residue was purified over silica gel column
  6. washeluted with methylene chloride (97%), methanol(2%), acetic acid(1%)

Sources & evidence

ORD record
ord-790a4dc4e5f746c1aec50c0d1472a357
Source dataset
uspto-grants-2004_08
Patent number
US06777421B2

Reaction notes

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