Acetaldehyde → HCID 68763137, compound

HRID 1398931Notes

Reaction equation

HRID 1398931 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([NH2:9])[C:3]=1[NH:10][CH2:11][CH2:12][CH2:13][OH:14].Cl.[Cl:16][C:17]1[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=1[CH:24]([OH:29])[C:25](=N)OC.[CH:30](=O)[CH3:31].[C:33](O[BH-](OC(=O)C)OC(=O)C)(=O)[CH3:34].[Na+]>C(O)C.C(=O)([O-])O.[Na+].CO>[Cl:16][C:17]1[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=1[CH:24]([OH:29])[C:25]1[N:10]([CH2:11][CH2:12][CH2:13][OH:14])[C:3]2[C:2]([N:1]([CH2:30][CH3:31])[CH2:33][CH3:34])=[CH:7][C:6]([F:8])=[CH:5][C:4]=2[N:9]=1

Participants

8

Reactant 4

HCID 177AcetaldehydeHCID 5049666Sodium triacetoxyborohydrideHCID 68735949HCID 68735949, compoundHCID 68736952HCID 68736952, compound

Product 1

HCID 68763137HCID 68763137, compoundYield 17.4%

Reagents, catalysts & solvents 3

HCID 702EthanolSolventHCID 887MethanolSolventHCID 516892Sodium BicarbonateSolvent

Procedure

A solution of 3-[(2,6-diamino-4-fluorophenyl)amino]propan-1-ol (498 mg, 2.50 mmol) and methyl 2-(2,4-dichlorophenyl)-2-hydroxyethanimidoate hydrochloride (812 mg, 3.00 mmol) in ethanol (5 mL) was stirred for 12 h at room temperature. The reaction mixture was diluted with aqueous sodium hydrogen carbonate, extracted with ethyl acetate, washed with brine, dried over sodium sulfate, filtrated, and concentrated in vacuo. The residue was dissolved in acetic acid (1.2 mL) and methanol (25 mL), and acetaldehyde (935 μL, 15.0 mmol) was added at 0° C. After 30 min, sodium triacetoxyborohydride (3.18 g, 15.0 mmol) was added. After 6 h, the reaction mixture was quenched with water, concentrated in vacuo, diluted with ethyl acetate, washed with aqueous sodium hydroxide (1 M) and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with a 10-50% ethyl acetate/n-hexane gradient mixture to give the title compound as a colorless solid (192 mg, 0.436 mmol, 17%).

Workup

  1. extractionextracted with ethyl acetate
  2. washwashed with brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltrated
  5. concentrationconcentrated in vacuo
  6. dissolutionThe residue was dissolved in acetic acid (1.2 mL)
  7. waitAfter 6 h
  8. customthe reaction mixture was quenched with water
  9. concentrationconcentrated in vacuo
  10. additiondiluted with ethyl acetate
  11. washwashed with aqueous sodium hydroxide (1 M) and brine
  12. dry with materialdried over sodium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated in vacuo
  15. customThe residue was purified by column chromatography on silica gel eluting with a 10-50% ethyl acetate/n-hexane gradient mixture

Sources & evidence

ORD record
ord-12db356220fa4cee9ee873ac1fd0701f
Source dataset
uspto-grants-2014_12
Patent number
US08901141B2

Reaction notes

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