HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1784300Erstellt: 24. Oktober 2026
Diisopropylcarbodiimide → methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-6-carboxylate
https://huagongshe.com/de/reaction/1784300
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylcarbodiimide | HCID 12734 | — |
| Edukt | 3,4,5-Trimethoxyphenyl isothiocyanate | HCID 118900 | — |
| Edukt | Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate | HCID 11962077 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | methyl 1-{3-[(tert-butoxycarbonyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-6-carboxylate | HCID 11962078 | 36% |
Reaktionsschritte
3,4,5-trimethoxyphenyl isothiocyanate (6.6 g, 1.2 eq) and diisopropylcarbodiimide (9.1 g, 3 eq) are successively added to a solution of methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate (7.75 g, 1 eq) in tetrahydrofuran (130 ml). The mixture is heated under reflux for 16 hours then cooled down to ambient temperature and concentrated under reduced pressure at 40° C. Water (100 ml) and dichloromethane (200 ml) are added to the residue obtained. After decantation and extractions, the combined organic phases are washed with salt water, dried over Na2SO4 then concentrated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent:heptane/ethyl acetate 8:2 to 3:7) produces the expected compound in the form of a solid which is washed with ether. (4.4 g; 36% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07501525B2 |
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| Quelldatensatz | uspto-grants-2009_03 |
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| ORD ID | ord-42067fc6e84247f4918deb5357125a06 |
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| Quellennotiz | uspto-grants-2009_03 |
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