Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,2'-Dipyridyl disulfide | HCID 65093 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Iminothiolane | HCID 433941 | — |
| Edukt | Cholesterol Ethylenediamine | HCID 69752158 | — |
| Edukt | Cholesterol ethylenediamine 2,2'-dipyridyldisulfide | HCID 131723204 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 178443924 | HCID 178443924 | — |
Reaktionsschritte
Pure cholesterol-ethylenediamine (10 mmol) was dissolved in 300 mL of DCM. 100 mmol of 2,2′-dipyridyl disulfide was dissolved in 100 mL of methanol and added to the cholesterol-ethylenediamine solution plus 20 mmol of diisopropylethylamine. 15 mmol of 2-iminothiolane was dissolved in 50 mL of methanol and then drop-wise added to the cholesterol-ethylenediamine/2,2′-dipyridyldisulfide solution over 30 minutes at R.T. Following an overnight R.T. stir, organic solvent was roto-evaporated away using medium vacuum until a minimal sample volume remained. Approximately 800 mL of acetonitrile was added to precipitate the crude product. The solid was then collected by filtration onto a Whatman #5 filter apparatus, rinsed several times with acetonitrile and then air-dried. The crude solid was dissolved in a minimal volume of chloroform and chromatographically purified using a silica column. The purified product presented a single TLC spot (4:1 chloroform/methanol), and a single peak (parent ion M+H=685) was identified by positive mode electrospray.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858226B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-8f7ab44c45384625abf6313842637ab3 |
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| Quellennotiz | uspto-grants-2005_02 |
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