HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N1-(S-(4-methoxybenzyl)thiosalicyloyl)-N4-benzylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | Benzoic acid, 2-[[(4-methoxyphenyl)methyl]thio]- | HCID 3568003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N1-(S-(4-methoxybenzyl)thiosalicyloyl)-N4-benzylpiperazine | HCID 69734254 | — |
Reaction Steps
N1-(S-(4-methoxybenzyl)thiosalicyloyl)-N4-benzylpiperazine (compound 5) was prepared using the same procedure described above using: 10 mM(2.743 g) of S-(4-methoxybenzyl) thiosalicylic acid, 3 mM(728 mg) of 1-Benzylpiperazine and 20 mM (3.525 g)triethylamine. The product was dissolved in 5 ml of methylene chloride and purified by column chromatography on a silica gel column (eluent: Ethyl acetate) to give 870 mg(20.1%) of a white crystal. The product was then further purified by crystallization from hexane. The purified product had having a melting point of 84-85° C. and had the following specifications:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541479B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-f3417361f43040a5b46b5b184243cb1d |
| Source note | uspto-grants-2003_04 |