HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-Piperazin-1-yl-4-thiophen-3-yl-[1,3,5]triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-(4-Thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 67387808 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Piperazin-1-yl-4-thiophen-3-yl-[1,3,5]triazine | HCID 67388017 | — |
Reaction Steps
To a 0° C. solution of 4-(4-thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester (60 mg, 0.17 mmol) in CH2Cl2 (2 mL) was added TFA (1 mL) dropwise. The resulting solution was allowed to warm to room temperature and stirred overnight. The resulting mixture was concentrated, then re-dissolved in CH2Cl2 and concentrated. The residue was dissolved in a mixture of CH2Cl2/MeOH (4:1, 5 mL), neutralized with Na2CO3, and stirred at room temperature for 30 min. The resulting solid was filtered, washed with CH2Cl2, and the filtrate was concentrated to yield a yellow gummy solid, which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022209B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-7e88ce7f175f4a058ceba29df95eaace |
| Source note | uspto-grants-2011_09 |