HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
tert-Butyl piperazine-1-carboxylate → 6-(4-Tert-butoxycarbonylpiperazin-1-ylsulfonyl)isoquinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 6-Aminoisoquinoline | HCID 588991 | — |
| Edukt | Isoquinoline-6-sulfonyl chloride | HCID 55280287 | — |
| Edukt | 6-(Piperazin-1-ylsulfonyl)isoquinoline dihydrochloride | HCID 66727131 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 6-(4-Tert-butoxycarbonylpiperazin-1-ylsulfonyl)isoquinoline | HCID 66727209 | — |
Reaktionsschritte
0.5 mL of triethylamine and 0.5 g of tert-butoxycarbonylpiperazine were added with stirring at room temperature to a dichloromethane solution (100 mL) of 6-chlorosulfonylisoquinoline (Reference Compound 2) synthesized according to Reference Example 2 from 500 mg of 6-aminoisoquinoline (Reference Compound 1), and reacted for 6 hours. After the completion of reaction, the reaction solution was washed with saturated saline and dried over anhydrous sodium sulfate. After concentration, the obtained crude product was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to obtain 150 mg of the compound of interest as a white crystal (23%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08951997B2 |
| Quelldatensatz | uspto-grants-2015_02 |
| ORD ID | ord-8a2892f9f65e4e048d3b0bd54c64f953 |
| Quellennotiz | uspto-grants-2015_02 |