HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 594384Erstellt: 26. Oktober 2026
Diisopropylethylamine → Methyl 5-(2,6-dimethoxyphenyl)-5-((quinolin-3-ylmethyl)amino)pentanoate
https://huagongshe.com/reaction/594384
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-Quinolinecarboxaldehyde | HCID 83641 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | Methyl 5-amino-5-(2,6-dimethoxyphenyl)pentanoate | HCID 69082713 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 5-(2,6-dimethoxyphenyl)-5-((quinolin-3-ylmethyl)amino)pentanoate | HCID 69082480 | — |
Reaktionsschritte
A solution of the chlorhydrate salt of methyl 5-amino-5-(2,6-dimethoxyphenyl)pentanoate (1.177 g; 3.87 mmol; 1.0 equiv.) in anh. DCE (24 ml) was treated successively with DIPEA (1.35 ml; 7.75 mmol; 2.0 equiv.), quinoline-3-carbaldehyde (609 mg; 3.87 mmol; 1.0 equiv.), and NaBH(OAc)3 (1.150 g; 5.42 mmol; 1.4 equiv.). The resulting beige heterogeneous mixture was further stirred at rt, under nitrogen, for 2 h 45 min. DCM (50 ml) and a solution of aq. sat. NaHCO3 (35 ml) were then added. The organic layer was further washed with a solution of aq. sat. NaHCO3 (35 ml) and with brine (35 ml). The resulting yellow organic layer was then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=10/1) afforded methyl 5-(2,6-dimethoxyphenyl)-5-((quinolin-3-ylmethyl)amino)-pentanoate as a yellow oil. LC-MS (conditions B): tR=0.66 min.; [M+H]+: 409.35 g/mol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242970B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-090ab0b42baf47889d987d836ecc4bdd |
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| Quellennotiz | uspto-grants-2016_01 |
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