L-(+)-Cysteine → S-(9H-Xanthen-9-yl)cysteine

HRID 19461

反応式

HRID 19461 の反応式
[NH2:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][SH:4].[CH:8]1[C:21]2[CH:20](O)[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[O:13][C:12]=2[CH:11]=[CH:10][CH:9]=1.C([O-])([O-])=O.[Na+].[Na+]>COCCOC.C(O)(C(F)(F)F)=O>[CH:8]1[C:21]2[CH:20]([S:4][CH2:3][C@@H:2]([C:5]([OH:7])=[O:6])[NH2:1])[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[O:13][C:12]=2[CH:11]=[CH:10][CH:9]=1

参加物

6

実験手順

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.

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 30 minutes
  2. concentrationThe mixture was then concentrated by rotary evaporation
  3. additionThe residue was diluted with 50 ml of water
  4. additionThe aqueous solution was treated with 10% aqueous citric acid solution
  5. stirringThe mixture was stirred at room temperature for 1 hr
  6. filtrationThe resultant white solid was collected by filtration
  7. washwas washed with 3×10 ml of water and 3×10 ml of ethyl acetate
  8. customThe product was dried

出典と根拠

ORDレコード
ord-946029af8d8640cf8e47831f71bc71c6
出典データセット
uspto-grants-2010_06
特許番号
US07745392B2

関連ノート

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