Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178472694 | HCID 178472694 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178514626 | HCID 178514626 | 80% |
Reaction Steps
A solution of 4.8 g of N2 -(2-phenoxathiinylsulfonyl)-L-arginyl-N-tetrahydrofurfurylglycine ethyl ester in 15 ml of methanol and 15 ml of 2N-NaOH solution was warmed to 40° C. and held at that temperature for 10 hours. At the end of this period, the reaction mixture was concentrated and chromatographed on 200 ml of Daiaion® SK 102 ion exchange resin (200-300 mesh, H+ form, manufactured by Mitsubishi Chemical Industries Limited) packed in water, washed with ethanol-water (1:4) and eluted with ethanol-water-NH4OH (10 : 9 : 1). The main fraction was evaporated to dryness and washed with ethyl ether to give 3.2 g (80 percent) of N2 -(2-phenoxathiinylsulfonyl)-L-arginyl-N-tetrahydrofurfurylglycine as an amorphous solid. I.R. (KBr): 3350, 1640, 1250 cm-1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04140681 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-8883017d45624f4aa93ddfb6f7388ac1 |
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| Source note | uspto-grants-1979_02 |
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