HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → Thiazolo[5,4-c]pyridine-2-carboxylic acid(1(r)-phenyl-ethyl)amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | Ethyl thiazolo[5,4-c]pyridine-2-carboxylate | HCID 14252940 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Thiazolo[5,4-c]pyridine-2-carboxylic acid(1(r)-phenyl-ethyl)amide | HCID 22980421 | — |
Reaction Steps
To a solution of thiazolo [5,4-c]pyridine-2-carboxylic acid ethyl ester (16 mg, 0.08 mmol) and 1(R)-phenyl ethyl amine (0.03 mL, 0.23 mmol) in dichloromethane(0.3 mL)was added a solution of trimethylaluminum in hexane(0.115 mL, 2.0 M., 0.23 mmol). The solution was then stirred for 5 hours at room temperature. After usual work-up, the product was purified by flash chromatography (CH2Cl2/EtOAc 1:1)and triturated in hexane to give 14 mg of the thiazolo derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06534520B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-79be83ba13ed4ceaa47ab1e0915013a7 |
| Source note | uspto-grants-2003_03 |