HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448781Erstellt: 24. Oktober 2026
L-Methioninol → N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol
https://huagongshe.com/de/reaction/448781
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | L-Methioninol | HCID 2724404 | — |
| Edukt | 2-[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one | HCID 57672803 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol | HCID 57672850 | 86% |
Reaktionsschritte
100 mg (0.74 mmol) of L-methioninol was added to a solution of 250 mg (0.68 mmol) of 2-[4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one in 20 ml of dimethylformamide. After the mixture was stirred at 80° C. for 15 hours, the reaction solution was concentrated under reduced pressure, ethyl acetate was added thereto, and the mixture was successively washed with water, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, and diisopropyl ether was added to the residue to wash the crystal to obtain 319 mg (86%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08481725B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-fa3326ca2b774c608a65c4913075f958 |
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| Quellennotiz | uspto-grants-2013_07 |
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