Triethylamine → 1-Methanesulfonyl-piperidine-4-carboxylic acid benzyl ester

HRID 2103989Notes

Reaction equation

HRID 2103989 reaction equation
Cl.[CH2:2]([O:9][C:10]([CH:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)=[O:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(N(CC)CC)C.[CH3:25][S:26](Cl)(=[O:28])=[O:27]>CN(C=O)C.O>[CH2:2]([O:9][C:10]([CH:12]1[CH2:17][CH2:16][N:15]([S:26]([CH3:25])(=[O:28])=[O:27])[CH2:14][CH2:13]1)=[O:11])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1

Participants

6

Reactant 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 68664822Benzyl piperidine-4-carboxylate hydrochloride

Product 1

HCID 574280631-Methanesulfonyl-piperidine-4-carboxylic acid benzyl esterYield 78%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

Piperidine-4-carboxylic acid benzyl ester, hydrochloride salt (1 g, 3.9 mmol, 1 e.) from step 3, was dissolved in DMF (15 ml), Triethylamine (0.55 ml, 4 mmol, 1 eq.) and methanesulfonylchloride were added. The mixture was stirred for 1 h at room temperature, then was poured in water (20 ml). The acqueous solution was extracted with Ethyl Acetate (90 ml) and the organic layer was dried over anhydrous sodium sulfate, evaporated under reduced pressure to give a colourless oil. Yield 78%, 0.9 g.

Workup

  1. extractionThe acqueous solution was extracted with Ethyl Acetate (90 ml)
  2. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  3. customevaporated under reduced pressure
  4. customto give a colourless oil

Sources & evidence

ORD record
ord-6eca5a8befd54937bb5e6c6f08129729
Source dataset
uspto-grants-2009_08
Patent number
US07576206B2

Reaction notes

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