Реакция #336805

Уравнение реакции

fluorescein isothiocyanate

Et3N

→

fluorescein

Растворители

DMF

CH2Cl2

Условия реакции

Обработка

1. 1
   ДругоеAn orange colored precipitate was immediately formed
2. 2
   Другоеremained during the entire period of the reaction
3. 3
   ДругоеAfter completion of the reaction
4. 4
   Фильтрацияthe insoluble precipitate was filtered off
5. 5
   Другоеand the solvent was removed under reduced pressure
6. 6
   workup.ADDITIONThe residue was diluted with CH2Cl2 (15 mL)
7. 7
   Промывкаwashed with 1N HCl (2×15 mL) and H2O (2×15 mL)
8. 8
   СушкаThe organic phase was dried over anhydrous Na2SO4
9. 9
   Другоеevaporated under reduced pressure

Методика

The starting amine (5) (0.15 g, 0.12 mmol) and fluorescein isothiocyanate (FLITC) (0.056 g, 0.14 mmol) were dissolved in a mixture of DMF and CH2Cl2 (6 mL, 1:5 ratio) at room temperature. The reaction was cooled to 0° C., and then an excess amount of Et3N (66 μL, 0.48 mmol) was added dropwise. An orange colored precipitate was immediately formed and remained during the entire period of the reaction. After completion of the reaction, the insoluble precipitate was filtered off; and the solvent was removed under reduced pressure. The residue was diluted with CH2Cl2 (15 mL), washed with 1N HCl (2×15 mL) and H2O (2×15 mL). The organic phase was dried over anhydrous Na2SO4 and evaporated under reduced pressure to afford 0.18 g (92%) of fluorescein-labeled guanidine (17) as an orange colored foam-shaped solid. 1H NMR (CD3OD): δ 8.20 (s, 1H, ArH), 7.86 (m, 1H, ArH), 7.22 (m, 2H, ArH), 6.64 (m, 3H, ArH), 6.56 (m, 2H, ArH), 3.86 (m, 2H, CH2NHCS), 3.66 (m, 12H, CH2O), 3.46 (m, 6H, CH2NHCO), 3.38 (m, 6H, CH2NH), 2.58 (m, 2H, CH2CO), 2.42 (m, 6H, CH2CO), 1.48 (s, 27H, t-Bu), 1.46 (s, 27H, t-Bu).

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