HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 3-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)piperidine-1-carboxylate → N-(2-(benzo[d]isothiazol-3-ylamino)ethyl)piperidine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 3-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)piperidine-1-carboxylate | HCID 11854495 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-(2-(benzo[d]isothiazol-3-ylamino)ethyl)piperidine-3-carboxamide | HCID 11856088 | 97.8% |
Reaction Steps
A solution of tert-butyl 3-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)piperidine-1-carboxylate (360 mg, 0.89 mmol) in trifluoroacetic acid (2 mL) and dichloromethane (2 mL) was cooled to 0° C. and stirred for 2 h. The reaction mixture was then concentrated under reduced pressure and lyophilized to yield N-(2-(benzo[d]isothiazol-3-ylamino)ethyl)piperidine-3-carboxamide as a yellow oil (265 mg). MW=304 confirmed by LC-MS, tr=2.39 min (Method B) MH+=305.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776847B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-a1e0bb617dd24cb98249043435ab0073 |
| Source note | uspto-grants-2010_08 |