Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Aminosalicylic Acid | HCID 4075 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Boc-Lys(Z)-OH | HCID 2724765 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Boc-Lys(Z)-OH | HCID 2724765 | 55% |
| Produkt | Ether isopropyl ether | HCID 21919906 | — |
Reaktionsschritte
70.4 g (0.14 mole) of BOC-L-Lys(Z)-SDP (m.w. 502.6) was dissolved in 200 ml of THF, which was then added dropwise to a solution of 21.4 g (0.14 mole) of 5-aminosalicylic acid (m.w. 153.14) in 187 ml of 1.5N NEM/DMF solution at 0°-5° C., and the reaction was effected at normal temperature for 18 hours, after which the reaction mixture was concentrated to 100-200 ml, 1600 ml of ether/ethyl acetate (50 v/50 v) was added, the mixture was washed with 1000 ml of cold 5% HCl three times and then with 1000 ml of saturated aqueous NaCl twice, active carbon was added, dried on magnesium sulfate, and the solvent was distilled off, to obtain, by recystallization from ether/isopropyl ether, 8.9 g (yield 55%) of crystalline BOC-L-Lys(Z)-CHA (m.w. 515.6) of m.p. 102°-105° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04605614 |
|---|
| Quelldatensatz | uspto-grants-1986_08 |
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| ORD ID | ord-94033bd2694a4121926a3cc0f69377af |
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| Quellennotiz | uspto-grants-1986_08 |
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