HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2080328Erstellt: 25. Oktober 2026
Diisopropylethylamine → 2-[4-(dimethylamino)phenyl]-N-{[3'-(1-piperazinylmethyl)-3-biphenylyl]methyl}acetamide
https://huagongshe.com/reaction/2080328
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-N,N-dimethylaminophenylacetic acid | HCID 152203 | — |
| Edukt | PyBOP | HCID 2724699 | — |
| Edukt | HCID 67101934 | HCID 67101934 | — |
| Lösungsmittel | Chloroform trifluoroacetic acid | HCID 19978452 | — |
| Produkt | 2-[4-(dimethylamino)phenyl]-N-{[3'-(1-piperazinylmethyl)-3-biphenylyl]methyl}acetamide | HCID 57736701 | 47,1% |
Reaktionsschritte
A mixture of PyBOP (0.08 mmol in 200 mL of DMF), {[3′-(1-piperazinylmethyl)-3-biphenylyl]methyl}amine (44 mmol in 200 mL of DMF) and DIPEA (30 mL) were added to [4-(dimethylamino)phenyl]acetic acid (0.07 mmol). The resulting mixture was stirred for 16 hours at room temperature, then the solvent was removed under vacuum. The residue was dissolved in methanol and purified by loading onto a SPE cartridge (SCX, 500 mg), washing with MeOH, and eluting with a 2 M solution of NH3 in MeOH. The NH3 fraction was collected and evaporated under vacuum to give a gum which was dissolved in 1:1 CHCl3/TFA (0.5 mL). After stirring for 2 hours, the solvent was removed under vacuum and the residue was dissolved in MeOH. The free base of the compound was obtained by loading the solution onto a SPE cartridge (SCX, 500 mg), washing with MeOH, and eluting with 2M NH3/MeOH. The ammonia fraction was collected and the solvent was removed under vacuum to give the title compound (14.6 mg). LC/MS: m/z, 443 (M+H), 2.21 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07932247B2 |
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| Quelldatensatz | uspto-grants-2011_04 |
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| ORD ID | ord-439de902695e460cb1ff45af2cd76549 |
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| Quellennotiz | uspto-grants-2011_04 |
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