Ethyl bromopyruvate → HCID 54238301, compound

HRID 1955038Notes

Reaction equation

HRID 1955038 reaction equation
[CH3:1][S:2]([NH:5][CH2:6][CH2:7][CH2:8][C:9]([NH2:11])=[S:10])(=[O:4])=[O:3].Br[CH2:13][C:14](=O)[C:15]([O:17][CH2:18][CH3:19])=[O:16]>CCO>[CH2:18]([O:17][C:15]([C:14]1[N:11]=[C:9]([CH2:8][CH2:7][CH2:6][NH:5][S:2]([CH3:1])(=[O:3])=[O:4])[S:10][CH:13]=1)=[O:16])[CH3:19]

Participants

4

Reactant 2

HCID 66144Ethyl bromopyruvate2×HCID 22246906HCID 22246906, compound

Product 1

HCID 54238301HCID 54238301, compoundYield 89.3%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A solution of 4-methanesulfonylamino-thiobutyramide (0.35 g, 1.8 mmol) and ethyl bromopyruvate (0.37 g, 1.9 mmol) in EtOH (50 mL) was stirred at room temperature for 17 h. Additional ethyl bromopyruvate (0.05 g, 0.26 mmol) was added and the reaction mixture was stirred at room temperature for 5.5 h. The reaction mixture was concentrated and was purified by flash chromatography (79:1 to 19:1 EtOAc:MeOH) to afford the title compound (0.47 g). 1H NMR (400 MHz, CDCl3) δ 8.05 (s, 1H), 4.40 (q, 2H), 3.24 (t, 2H), 3.17 (t, 2H), 2.96 (s, 3H), 2.10 (t, 2H), 1.39 (t, 3H); MS 293 (M+ +1).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. customwas purified by flash chromatography (79:1 to 19:1 EtOAc:MeOH)

Sources & evidence

ORD record
ord-c03d7cdee7594fe0ae548895de0447cc
Source dataset
uspto-grants-2000_09
Patent number
US06124314

Reaction notes

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