HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → HCID 68835224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | p-Toluenesulfonyl isocyanate | HCID 77703 | — |
| Reactant | HCID 68836927 | HCID 68836927 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68835224 | HCID 68835224 | — |
Reaction Steps
The material produced in Step 1 (0.78 g, 2.0 mmol) was split into three batches. Each batch was suspended in DMF (3 mL) and then TsNCO (0.3 ml, 2 mmol) was added. The reaction mixture was stirred at rt overnight. Ethylamine (3 ml of a 2 M solution in THF, 6 mmol) was added and the resulting mixture was irradiated with microwaves at 130° C. for 40 minutes. The three batches were combined, filtered, washed with THF, and dried to afford 4-[2-(3-ethyl-ureido)-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl]-piperazine-1-carboxylic acid tert-butyl ester as a solid. MS (APCI+) 467 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524860B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-77dce7dc2eac443093005091dc1823f6 |
| Source note | uspto-grants-2009_04 |