HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 19071138, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methyl 3-(piperazin-1-yl)propanoate | HCID 15343154 | — |
| Reactant | HCID 136351310 | HCID 136351310 | — |
| Reactant | HCID 136482112 | HCID 136482112 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19071138 | HCID 19071138 | — |
Reaction Steps
1.13 g of 3-[2-(1-(5-oxo-1,2,4-oxadiazolin-3-yl)-4-piperazinyl)ethyl]-5-[4-(2-carboxyethyl)piperazino]methyloxazolidin-2-one [obtainable according to Ex. 1 by reaction of methyl 3-piperazinopropanoate with 3-[2-(1-(5-oxo-1,2,4-oxadiazolin-3-yl)-4-piperazinyl)ethyl]-5-methanesulfonylmethyloxazolidin-2-one and subsequent hydrolysis of the product] are dissolved in 50 ml of methanol and hydrogenated on Raney Nickel. The reaction mixture is then filtered and the filtrate is concentrated in vacuo. The product obtained is treated with 20 ml of ethyl acetate in the presence of heat and filtered off with suction after cooling. 3-[2-(1-Amidino-4-piperazinyl)ethyl]-5-[4-(2-carboxyethyl)piperazino]methyloxazolidin-2-one is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05776937 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-6aeafc7daa3e4b2bbb30bbe44f5a3dd1 |
| Source note | uspto-grants-1998_07 |