HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 10150892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Methyl (1,3-benzothiazol-2-yl)acetate | HCID 358756 | — |
| Reactant | HCID 11470752 | HCID 11470752 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10150892 | HCID 10150892 | 55% |
Reaction Steps
200 mg (0.793 mmol) 4-[4-(2-Fluoro-ethyl)-piperazin-1-yl]-2-hydroxy-benzaldehyde and 164 mg (1 eq.) benzothiazol-2-yl-acetic acid methyl ester are heated to reflux for 3 h in 5 mL benzene and 2.5 mL acetonitrile, in the presence of 0.157 mL (2 eq.) piperidine. The reaction mixture is allowed to reach room temperature and the precipitate filtered off, washed with diethylether and dried under high vacuum to yield 90 mg (55%) of desired product as a yellow powder (melting point: 246° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07569337B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-18eefd571c03425384bca27ebde444a8 |
| Source note | uspto-grants-2009_08 |