Sodium Carbonate → HCID 22248142, compound

HRID 890075Notes

Reaction equation

HRID 890075 reaction equation
[CH3:1][O:2][C:3]1[C:4]([CH:9]=O)=[N:5][CH:6]=[CH:7][N:8]=1.Cl.[O:12]1[C:16]2[C:17]([CH2:21][CH2:22][CH:23]3[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]3)=[CH:18][CH:19]=[CH:20][C:15]=2[CH:14]=[CH:13]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)([O-])[O-].[Na+].[Na+]>C(OCC)(=O)C.O1CCCC1>[O:12]1[C:16]2[C:17]([CH2:21][CH2:22][CH:23]3[CH2:28][CH2:27][N:26]([CH2:9][C:4]4[C:3]([O:2][CH3:1])=[N:8][CH:7]=[CH:6][N:5]=4)[CH2:25][CH2:24]3)=[CH:18][CH:19]=[CH:20][C:15]=2[CH:14]=[CH:13]1

Participants

7

Procedure

After adding 124 mg of 3-methoxypyrazine-2-carboxaldehyde and 200 mg of 4-[2-(benzofuran-7-yl)ethyl]piperidine hydrochloride to 3 ml of tetrahydrofuran, 238 mg of sodium triacetoxyborohydride was added and the mixture was stirred overnight at room temperature. Aqueous sodium carbonate solution was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was washed with water and saturated brine in that order and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (218 mg, 82% yield).

Workup

  1. additionwas added
  2. washThe organic layer was washed with water and saturated brine in that order
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate)

Sources & evidence

ORD record
ord-6f6e5b7185d447ab89fcc3ea55389afd
Source dataset
uspto-grants-2006_02
Patent number
US06995144B2

Reaction notes

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