Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86753090 | HCID 86753090 | — |
| Product | HCID 10066640 | HCID 10066640 | 45.7% |
Reaction Steps
A mixture of 0.75 g of methyl [8-(3-methylureido)-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]-indeno[1,2-e]pyrazin-10-yl]acetate and 4 ml of 1N sodium hydroxide is heated at a temperature in the region of 35° C. for 2 hours. The mixture is acidified with 1N hydrochloric acid and the precipitate formed is filtered off, washed with distilled water and dried at 60° C. under vacuum (1 mmHg; 0.13 kPa). 0.33 g of [8-(3-methylureido)-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]-indeno[1,2-e]pyrazin-10-yl]acetic acid is obtained in the form of a yellow solid melting above 260° C. (Analysis, % calculated C: 57.79, H: 4.28, N: 19.82, O: 18.11, % found C: 57.8, H: 4.3, N: 19.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807859 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-8acbaba83b8047cd8b5a356384d29e40 |
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| Source note | uspto-grants-1998_09 |
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