Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | HCID 22992371 | HCID 22992371 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15574323 | HCID 15574323 | — |
Reaction Steps
To a solution of 5-chloro-4-nitro-2,1,3-thiadiazole (1.0 g, 4.64 mmol) in anhydrous NMP (5 ml) was added triethylamine (0.65 ml, 4.64 mmol) and benzylamine (0.51 ml, 4.64 mmol). The mixture was heated to 80° C. for 1 hour. The cooled mixture was poured into ice-water (50 ml) and the product was filtered off, washed with water and dried. Yield: 1 g (75%). This product (0.5 g, 1.75 mmol) was suspended in ethanol (20 ml) and hydrogenated at ambient pressure using palladium (5% on activated carbon) as the catalyst. Yield: quantitative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06624186B2 |
|---|
| Source dataset | uspto-grants-2003_09 |
|---|
| ORD ID | ord-7c29bc13772c42acb2c65808376d7e4b |
|---|
| Source note | uspto-grants-2003_09 |
|---|