HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → N-[1-(1-methyl-1H-pyrazol-4-yl)ethyl]ethane-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(1-methyl-1H-pyrazol-4-yl)ethan-1-one | HCID 3596939 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[1-(1-methyl-1H-pyrazol-4-yl)ethyl]ethane-1,2-diamine | HCID 14009898 | 48.1% |
Reaction Steps
1-(1-Methyl-1H-pyrazol-4-yl)-ethanone (250 mg) and ethylenediamine (362 mg) were dissolved in methanol (10 ml), the solution was added with acetic acid (1.21 g) and sodium cyanoborohydride (189 mg), and the mixture was stirred at room temperature for 48 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate and tetrahydrofuran, the layers were separated, and then the organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol:28% aqueous ammonia=10:1:0.1) to obtain the title compound (163 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097708B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-c448b2dc18304b66a020f37dce9cbb5a |
| Source note | uspto-grants-2012_01 |