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Triethylamine → 3-(2-Acetamidoethylthio)-2-oxoglutaric acid

HRID 232218
Notes
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Reaction equation

HRID 232218 reaction equation
Br[CH:2]([CH2:8][C:9]([OH:11])=[O:10])[C:3](=[O:7])[C:4]([OH:6])=[O:5].[C:12]([NH:15][CH2:16][CH2:17][SH:18])(=[O:14])[CH3:13].C(N(CC)CC)C>ClCCl>[C:12]([NH:15][CH2:16][CH2:17][S:18][CH:2]([CH2:8][C:9]([OH:11])=[O:10])[C:3](=[O:7])[C:4]([OH:6])=[O:5])(=[O:14])[CH3:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 14484AcetylcysteamineHCID 1959343-Bromo-2-ketoglutarate

Product 1

HCID 200308993-(2-Acetamidoethylthio)-2-oxoglutaric acidYield 60.7%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

In 20 ml of dichloromethane was suspended 1.0 g of 3-bromo-2-oxoglutaric acid. To the suspension was added, while stirring under ice-cooling, 0.5 g of 2-acetamidoethanethiol, followed by addition of 1.83 ml of triethylamine. The reaction solution was stirred at room temperature for one hour, then the solvent was evaporated off. To the residue were added ethyl acetate and water. The aqueous layer was taken, which was adjusted to pH 1~2 with 1N-HCl, followed by extraction with ethyl acetate. The extract solution was washed with water and dried (MgSO4), followed by evaporating off the solvent to give 0.67 g of 3-(2-acetamidoethylthio)-2-oxoglutaric acid as a pale yellow oily product. To this product were added, while stirring under ice-cooling, 0.32 ml of dicyclohexylamine and 0.34 g of 4-nitrobenzyl bromide. The reaction solution was stirred for 15 hours at room temperature, followed by dilution with ethyl acetate. The crystals which separated out were filtered off, and the filtrate was washed with water and dried (MgSO4), followed by evaporating off the solvent. The residue was subjected to a silica gel column chromatography, followed by elution with ethyl acetate then with ethyl acetate--acetic acid (100:3) to give 0.4 g of the subject Compound (70) as a pale yellow oily product.

Workup

  1. additionTo the suspension was added
  2. temperaturecooling
  3. stirringThe reaction solution was stirred at room temperature for one hour
  4. customthe solvent was evaporated off
  5. additionTo the residue were added ethyl acetate and water
  6. extractionfollowed by extraction with ethyl acetate
  7. washThe extract solution was washed with water
  8. dry with materialdried (MgSO4)
  9. customby evaporating off the solvent

Sources & evidence

ORD record
ord-9fa1a7c82e8e4990be6c2819dd3a8524
Source dataset
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04851422

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes