HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22101205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 15703582 | HCID 15703582 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22101205 | HCID 22101205 | — |
Reaction Steps
To a solution of 3-amino-1benzyl-4-ethoxycarbonylpyrazole (0.5 g) in DMF (10 ml), was added 60% NaH (0.082 g). After stirring for 5 min at room temperature, benzyl bromide (0.307 ml) was added, and the mixture was stirred for 1 h at room temperature. The reaction mixture was evaporated under reduced pressure followed by silica-gel column chromatography (toluene/ ethyl acetate=50/1) to give 3-benzylamino-1-benzyl-4-ethoxycarbonylpyrazole (0.3 g). This intermediate was derived to the title compound by the similar method to Reference Example 1 (yield 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849779 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-34177f4873c046c29d199d60c6a594fb |
| Source note | uspto-grants-1998_12 |