Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178513233 | HCID 178513233 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68630757 | HCID 68630757 | 94.5% |
Reaction Steps
To a stirred solution of acetic acid (30 mg, 0.5 mmol) in acetonitrile (2.15 ml) was added at room temperature 1-hydroxy-benzotriazole (95 mg, 0.6 mmol) and N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimid-hydrochloride (110 mg, 0.57 mmol). The mixture was allowed to stir for 3 h at room temperature and N-hydroxy-2-((R)-indan-1-ylamino)-quinoline-6-carboxamidine (107 mg, 0.34 mmol) was added together with acetonitrile (2.15 ml). The mixture was allowed to stir for 2 h at room temperature, evaporated to dryness and diluted with acetic acid (3.5 ml). The reaction mixture was allowed to stir for 2 h at 100° C., evaporated, poured into saturated NaHCO3 solution (40 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with brine (2×50 ml), dried (MgSO4) and evaporated. The crude product was purified by flash chromatography (ethyl acetate/heptane) on silica gel and crystallization (ethyl acetate/heptane) to yield the title compound as light yellow oil (110 mg, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188284B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-8cf315acbc9d4331913d0a6ff6580641 |
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| Source note | uspto-grants-2012_05 |
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