HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 2-(ethoxycarbonyloxymethyl)-5-(4,5-di-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate → ethyl 5-(2-amino-4,5-dimethoxybenzoyl)-2-(ethoxycarbonyloxymethyl)-2H-1,2,3-triazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 2-(ethoxycarbonyloxymethyl)-5-(4,5-di-methoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate | HCID 12051530 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl 5-(2-amino-4,5-dimethoxybenzoyl)-2-(ethoxycarbonyloxymethyl)-2H-1,2,3-triazole-4-carboxylate | HCID 12051531 | 95.2% |
Reaction Steps
Ethyl 2-(ethoxycarbonyloxymethyl)-5-(4,5-dimethoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate (45 mg) prepared in step (3a) was dissolved in ethyl acetate (1 ml). Palladium hydroxide (15 mg) was added to the solution. The mixture was stirred in a hydrogen atmosphere at room temperature for 15 hr. The reaction solution was filtered through Celite. The filtrate was concentrated under reduced pressure to give ethyl 5-(2-amino-4,5-dimethoxybenzoyl)-2-(ethoxycarbonyloxymethyl)-2H-1,2,3-triazole-4-carboxylate as a yellow oil (40 mg, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06372735B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-4499bcb9c5f946f1bd77c21842e3222b |
| Source note | uspto-grants-2002_04 |