HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178465650, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178511206 | HCID 178511206 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178465650 | HCID 178465650 | 40.6% |
Reaction Steps
A mixture of 5-chloro-3-{[4-[N-(p-nitrobenzyloxycarbonyl)acetimidoylamino]-1-piperazinyl]carbonylmethyl}-2-benzothiazolinone (2.0 g), acetic acid (0.3 ml), water (3 ml), 10% palladium on carbon (2.0 g) in tetrahydrofuran (40 ml) and methanol (20 ml) was incubated under an atmosphere of hydrogen for 3 hours. Palladium on carbon was filtered off, and the filtrate was coevaporated with ethanol. The residue obtained was purified by aluminum column chromatography, treated with hydrogen chloride in ethanol, and recrystallized from a mixture of water, ethanol and ether to give yellow crystals of 5-chloro-3-[(4-acetimidoylamino-1-piperazinyl)carbonylmethyl]-2-benzothiazolinone hydrochloride (0.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04797399 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-282ed1c773e14086aa001a16e29ea169 |
| Source note | uspto-grants-1989_01 |