HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl-piperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-[Methyl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amino]-piperidine-1-carboxylic acid benzyl ester | HCID 59323570 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl-piperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine | HCID 59323568 | 93% |
Reaction Steps
A solution of 4-[M ethyl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amino]-piperidine-1-carboxylic acid benzyl ester (D1) (0.91 g, 2.27 mmol) in a solution 6 N of hydrochloric acid (15 ml) was stirred at 150° C. for 10 min., under microwave irradiation. After cooling to room temperature, the reaction mixture was diluted with water and extracted with dichloromethane (25 ml). The aqueous layer was basified with a saturated solution of sodium carbonate and extracted with dichloromethane (3×25 ml). The combined organic extracts were dried (Na2SO4) and the solvent evaporated in vacuo to yield D2 (0.56 g, 93%) as a solid. C9H13F3N4S requires 266. Found 266 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933101B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-cd163e0a52b04b64966deef784f17112 |
| Source note | uspto-grants-2015_01 |