Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 56637010 | HCID 56637010 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 18958846 | HCID 18958846 | 84.2% |
Reaction Steps
2.5 g of 2- {[4 - {[7 -n-propyl-5-methyl- 3-oxo-2-(ethoxycarbonylmethyl)-2,3-dihydro-1,2,4-triazolo[4,3-c]-pyrimidin- 8-Yl]methyl}phenyl]aminocarbonyl}benzenesulphonic acid, prepared in Example 34, are dissolved in 30 ml of water containing 1 g of sodium hydroxide. The mixture is heated to 60° C. for 2 hours, cooled and acidified with hydrochloric acid to give 2 g of 2-{[4-{[7-n-propyl-5-methyl-3-oxo-2-(carboxymethyl)-2,3-dihydro-1,2,4-triazolo[4,3-c]pyrimidin-8-yl]methyl}phenyl]-aminocarbonyl}benzenesulphonic acid in the form of crystals of melting point 296°-300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05358950 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-3587e7b3deb44524be296e4bb4ef55a5 |
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| Source note | uspto-grants-1994_10 |
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