HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23023993, compound → HCID 23023940, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23023993 | HCID 23023993 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23023940 | HCID 23023940 | 99% |
Reaction Steps
To a suspension of methyl 4-(N-methyl-N-(4-(4-nitrophenyl)-2-thiazolyl)aminomethyl)benzoate (200.0 g, 0.522 mol) obtained in Example 1(3) in a mixture of ethanol (800 ml, 4.0 v/w) and tetrahydrofuran (800 ml, 4.0 v/w) was added 10% palladium carbon (20.0 g) and the mixture was stirred overnight under a hydrogen atmosphere at 3 atm. The reaction mixture was filtered through celite and 10% palladium carbon (20.0 g) was added to the filtrate. The mixture was stirred under a hydrogen atmosphere at 3 atm for 3 hr. After celite filtration and solvent evaporation, toluene (800 ml) was added to the residue and the solvent was evaporated to give the title compound (182.5 g, yield 99.0%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07163952B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-1415eb6a097847278ff7ec504d7413a3 |
| Source note | uspto-grants-2007_01 |