Reacción #47739

ord-946029af8d8640cf8e47831f71bc71c6

Ecuación de reacción

N[C@@H](CS)C(=O)O
cysteine
OC1c2ccccc2Oc2ccccc21
9H-xanthen-9-ol
O=C([O-])[O-].[Na+].[Na+]
Na2CO3
N[C@@H](CSC1c2ccccc2Oc2ccccc21)C(=O)O
product
Rendimiento 86.3%
N[C@@H](CSC1c2ccccc2Oc2ccccc21)C(=O)O
S-(9H-Xanthen-9-yl)cysteine
Rendimiento 86.3%

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe reaction mixture was stirred at room temperature for 30 minutes
  2. 2
    ConcentraciónThe mixture was then concentrated by rotary evaporation
  3. 3
    workup.ADDITIONThe residue was diluted with 50 ml of water
  4. 4
    workup.ADDITIONThe aqueous solution was treated with 10% aqueous citric acid solution
  5. 5
    workup.STIRRINGThe mixture was stirred at room temperature for 1 hr
  6. 6
    FiltraciónThe resultant white solid was collected by filtration
  7. 7
    Lavadowas washed with 3×10 ml of water and 3×10 ml of ethyl acetate
  8. 8
    OtroThe product was dried

Procedimiento

A sample of 0.61 g of cysteine (5 mmole) was suspended in 100 ml of 1,2-dimethoxyethane and 2 ml of TFA. The suspension was stirred under nitrogen gas at room temperature until the solution became clear. To this clear solution was added 1 g of 9H-xanthen-9-ol (5.1 mmole) in one portion. The reaction mixture was stirred at room temperature for 30 minutes and was then neutralized to pH 7 by the addition of a saturated aqueous Na2CO3 solution. The mixture was then concentrated by rotary evaporation. The residue was diluted with 50 ml of water. The aqueous solution was treated with 10% aqueous citric acid solution to adjust the pH to 6. The mixture was stirred at room temperature for 1 hr. The resultant white solid was collected by filtration and was washed with 3×10 ml of water and 3×10 ml of ethyl acetate. The product was dried to yield 1.30 g of product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745392B2uspto-grants-2010_06