HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Fluoride → {5-Amino-1-[2-(trityloxy)ethyl]pyrazol-4-yl}methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Fluoride | HCID 5235 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 5-Amino-1-[2-(trityloxy)ethyl]pyrazole-4-carbonitrile | HCID 17962018 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {5-Amino-1-[2-(trityloxy)ethyl]pyrazol-4-yl}methylamine | HCID 17961999 | 77.2% |
Reaction Steps
To a suspension of lithium aluminum hydride (4.89 g, 129 mmol) in tetrahydrofuran (318 ml) was added 5-amino-1-[2-(trityloxy)ethyl]pyrazole-4-carbonitrile (25.4 g, 64.4 mmol) at room temperature. The mixture was stirred under reflux for 12 hours. After cooling on an ice bath, sodium fluoride (25.4 g), tetrahydrofuran (100 ml), dichloromethane (200 ml) and water (10 ml) were added to the reaction mixture. The insoluble materials were removed by filtration. The filtrate was concentrated in vacuo to give {5-amino-1-[2-(trityloxy)ethyl]pyrazol-4-yl}methylamine (19.8 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179801B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-a7c864b5051d44e0947db4cbc9ed8918 |
| Source note | uspto-grants-2007_02 |