Ethyl oxoacetate → HCID 66941718, compound

HRID 2267226Notes

Reaction equation

HRID 2267226 reaction equation
[CH3:1][C:2]1([N:8]2[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]2)[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.O=[CH:22][C:23]([O:25][CH2:26][CH3:27])=[O:24].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C([O-])(O)=O.[Na+]>C1COCC1>[CH2:26]([O:25][C:23]([CH2:22][N:5]1[CH2:6][CH2:7][C:2]([N:8]2[CH2:9][CH2:10][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:12][CH2:13]2)([CH3:1])[CH2:3][CH2:4]1)=[O:24])[CH3:27]

Participants

6

Procedure

A mixture of 1.53 g (4.78 mmol) tert-butyl 4-(4-methyl-piperidin-4-yl)-piperazine-1-carboxylate and 1.1 mL (5.55 mmol) ethyl oxo-acetate (50% in toluene) in 50 mL THF was stirred for 1 h at RT. The reaction mixture was cooled to 0° C., 1.25 g (5.90 mmol) sodium triacetoxyborohydride was added batchwise and after elimination of the cooling bath the mixture was stirred overnight at RT. It was combined with 10 mL 20% NaHCO3 solution, extracted exhaustively with EtOAc and the combined organic phases were dried over Na2SO4. After elimination of the desiccant and solvent the residue was purified by chromatography (Alox, DCM/EtOH 100:1).

Workup

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. stirringafter elimination of the cooling bath the mixture was stirred overnight at RT
  3. extractionextracted exhaustively with EtOAc
  4. dry with materialthe combined organic phases were dried over Na2SO4
  5. customAfter elimination of the desiccant and solvent the residue was purified by chromatography (Alox, DCM/EtOH 100:1)

Sources & evidence

ORD record
ord-7ce159bdb37148d688f2991dcef24fb2
Source dataset
uspto-grants-2010_12
Patent number
US07858622B2

Reaction notes

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