HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(3-Nitro-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine → 5-(3-Amino-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(3-Nitro-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine | HCID 67042802 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(3-Amino-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine | HCID 69927552 | 68.9% |
Reaction Steps
To a solution of 5-(3-nitro-benzyl)-[1,2,4]triazolo[1,5-c]quinazolin-2-ylamine (0.10 g, 0.31 mmol), prepared as described in Example 2, in N,N-dimethylformamide (10 mL), 10% Pd/C (50% w/w, 0.05 g) was added. The mixture was reacted in Parr Apparatus at 40 p.s.i. for 5 h. The suspension was filtered through Celite®. After washing the filter with methanol, the solution was evaporated to dryness. The crude was twice crystallized from ethyl acetate to provide the title product (0.062 g, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580783B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-749b572815d34ab989a5d2dd2c7e4ac1 |
| Source note | uspto-grants-2013_11 |