Reaktionsgleichung
[C:1]1(CCCC(NN)=O)[C:14]2[C:15]3=[C:16]4[C:11](=[CH:12][CH:13]=2)[CH:10]=[CH:9][CH:8]=[C:7]4[CH:6]=[CH:5][C:4]3=[CH:3][CH:2]=1.OC1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O>CS(C)=O>[CH:8]1[C:7]2[C:16]3=[C:15]4[C:4](=[CH:5][CH:6]=2)[CH:3]=[CH:2][CH:1]=[C:14]4[CH:13]=[CH:12][C:11]3=[CH:10][CH:9]=1Komponenten
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
10 μl of a solution containing 400 nmol of 1-pyrenebutanoic acid, hydrazide (Molecular Probes) in DMSO was added to 50 nmol of lactose which had been dried adequately, and lactose was fully dissolved by sonication. 1 μl of acetic acid was added thereto and the mixture was stirred adequately. The reaction mixture was then heated at 90° C. for 1 hour. After the reaction mixture was dried using a centrifugation concentrator, 10 μl of a solution containing 2.5 M borane-dimethylamine complex and 30% acetic acid in DMSO was added to the residue, and the residue was fully dissolved by sonication. The mixture was then heated at 80° C. for 1 hour. The reaction mixture was dried using a centrifugation concentrator. The residue was re-dissolved in 50% acetonitrile and purified using normal phase high performance liquid chromatography. The molecular weight of the purified pyrene-labeled lactose was determined using a triple-quadrupole ion-spray mass-spectrometer API-300. As a result, a positive molecular ion (629.3) was observed.
Aufarbeitung
- customhad been dried adequately
- dissolutionlactose was fully dissolved by sonication
- addition1 μl of acetic acid was added
- customAfter the reaction mixture was dried
- additioncontaining 2.5 M borane-dimethylamine complex and 30% acetic acid in DMSO
- additionwas added to the residue
- dissolutionthe residue was fully dissolved by sonication
- temperatureThe mixture was then heated at 80° C. for 1 hour
- customThe reaction mixture was dried
- dissolutionThe residue was re-dissolved in 50% acetonitrile
- custompurified
Quellen und Nachweise
- ORD-Eintrag
- ord-826ed366131548acb6b3e46ab7bfbc01
- Quelldatensatz
- uspto-grants-2005_07
- Patentnummer
- US06916920B2
Verknüpfte Notizen
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