HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dimethyl-2-imidazolidinone → HCID 22120656, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | HCID 22120584 | HCID 22120584 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178420936 | HCID 178420936 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22120656 | HCID 22120656 | 69.1% |
Reaction Steps
N-(4-Pyridyl)-2-benzyloxy-4-tert-butoxycarbonylaminomethylbenzamide (3.38 g) was subjected to catalytic reduction using 10% palladium hydroxide carbon (1 g) in a solution of ethanol (10 ml) and dimethylimidazolidinone (70 ml) in a stream of hydrogen. After the reaction, the catalyst was removed by filtration, and the mixture was concentrated under reduced pressure to give 1.85 g of N-(4-pyridyl)-4-tert-butoxycarbonylaminomethyl-2-hydroxybenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958944 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-99656effc1d542f1bc3d6126340acf02 |
| Source note | uspto-grants-1999_09 |