Sodium Hydroxide → HCID 22248055, compound

HRID 606210Notes

Reaction equation

HRID 606210 reaction equation
[CH3:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1/[CH:7]=[CH:8]/[CH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1.[CH3:15][O:16][C:17]1[C:18]([CH:23]=O)=[N:19][CH:20]=[CH:21][N:22]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>O1CCCC1>[CH3:15][O:16][C:17]1[C:18]([CH2:23][N:12]2[CH2:13][CH2:14][CH:9](/[CH:8]=[CH:7]/[C:3]3[S:4][CH:5]=[CH:6][C:2]=3[CH3:1])[CH2:10][CH2:11]2)=[N:19][CH:20]=[CH:21][N:22]=1

Participants

6

Procedure

After dissolving 139 mg of (E)-4-[2-(3-methyl-2-thienyl)vinyl]piperidine in 7 ml of tetrahydrofuran, 111 mg of 3-methoxypyrazine-2-carboxaldehyde and 213 mg of sodium triacetoxyborohydride were added while stirring, and the stirring was continued overnight at room temperature. A 1N sodium hydroxide solution was added to the reaction mixture to render it alkaline, and then extraction was performed with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (120 mg, 54% yield).

Workup

  1. additionwere added
  2. extractionextraction
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. customThe residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate)

Sources & evidence

ORD record
ord-5177d92175444d23be79e90e86c6a55f
Source dataset
uspto-grants-2011_03
Patent number
US07915274B2

Reaction notes

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