Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178512836 | HCID 178512836 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178514624 | HCID 178514624 | 87% |
Reaction Steps
To a solution of 3.00 g of NG -nitro-N2 -(5,6,7,8-tetrahydro-2-naphthylsulfonyl)-L-arginyl-N-cyclohexylmethylglycine benzyl ester in 50 ml of ethanol and 0.5 ml of acetic acid was added 0.5 g of palladium-black and then the mixture was shaken in a hydrogen atmosphere for 100 hours at room temperature. At the end of this period, the ethanol solution was filtered to remove the catalyst and evaporated to dryness. The residue was washed several times with dry diethyl ether and chromatographed on 80 ml of Daiaion® SK 102 ion exchange resin (200-300 mesh, H+ form, manufactured by Mitsubishi Chemical Industries Limited) packed in water, washed with water and eluted with 3% ammonium hydroxide solution. The fraction eluted from 3% ammonium hydroxide solution was evaporated to dryness to give 2.07 g (87%) of N2 -(5,6,7,8-tetrahydro-2-naphthylsulfonyl)-L-arginyl-N-cyclohexylmethylglycine as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04072743 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-511bd8e2967a40eca533aae6c45725a9 |
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| Source note | uspto-grants-1978_02 |
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