Acetic Acid → HCID 86724913, compound
Reaction equation
[C:1](O)(=O)[CH3:2].[NH:5]1[CH2:15][CH2:14][CH:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:7][CH2:6]1.C(O[BH-](O[C:26](=[O:28])[CH3:27])OC(=O)C)(=O)C.[Na+].[C:30](=[O:33])(O)[O-].[Na+]>ClCCl>[CH2:12]([O:11][C:9]([CH:8]1[CH2:7][CH2:6][N:5]([CH:2]2[CH2:1][CH2:15][N:5]([C:30]([O:28][CH2:26][CH3:27])=[O:33])[CH2:6][CH2:7]2)[CH2:15][CH2:14]1)=[O:10])[CH3:13]Participants
Conditions
- Temperature
- 0 °C
Procedure
A mixture of ethyl 4-oxo piperidine-1-carboxylate (3.14 grams, 18.3 mmol, obtained in the above step) in acetic acid (1.05 mL, 18.3 mmol) was added to a stirred solution of ethyl isonipecotate (2.87 mL, 18.3 mmol) in dichloromethane (10 mL) cooled at 0° C. Solid sodium triacetoxy borohydride (11.6 grams, 54.9 mmol) was added portion wise over a period of 15 minutes. The reaction mixture was gradually warmed to room temperature and stirred for 16 hours. The reaction mixture was cooled to 0° C. and basified with saturated sodium bicarbonate solution (pH 7.5). The two layers were separated, the organic layer was washed with brine, dried over anhydrous sodium sulfate and the volatiles were removed under reduced pressure. The crude product was purified by silica gel column chromatography to obtain [1,4′]Bipiperidinyl-4,1′-dicarboxylic acid diethyl ester (5.51 grams).
Workup
- temperatureThe reaction mixture was gradually warmed to room temperature
- customThe two layers were separated
- washthe organic layer was washed with brine
- dry with materialdried over anhydrous sodium sulfate
- customthe volatiles were removed under reduced pressure
- customThe crude product was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-885d7747693042929cc3da3343624fe0
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09079894B2
Reaction notes
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