HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → ethyl (2S)-1-(1,3-benzothiazol-2-yl)-2-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2-Chlorobenzothiazole | HCID 11987 | — |
| Reactant | Ethyl (2S)-2-piperidinecarboxylate | HCID 736055 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | ethyl (2S)-1-(1,3-benzothiazol-2-yl)-2-piperidinecarboxylate | HCID 57016205 | 81.9% |
Reaction Steps
2-Chloro-1,3-benzothiazole (503 mg) was added to a suspension of ethyl (2S)-2-piperidinecarboxylate (471 mg) [J.A.C.S. (1993), 115(22), 9925-9938], triethylamine hydrochloride (414 mg) and copper powder (38 mg) in xylene (5 ml). The reaction mixture was refluxed for 28 hours, after which time ethyl acetate (20 ml) was added to the cooled mixture and the solids filtered off. The organic layer was washed with water, dried over magnesium sulphate and the solvent removed under reduced pressure to afford ethyl (2S)-1-(1,3-benzothiazol-2-yl)-2-piperidinecarboxylate (705 mg) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562964B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-dc04ecab06f84771aa20652422f9cdc2 |
| Source note | uspto-grants-2003_05 |