Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-(Isoquinolin-5-ylamino)-4-ethoxy-cyclobut-3-ene-1,2-dione | HCID 10801832 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15228051 | HCID 15228051 | 77% |
Reaction Steps
A suspension of the the product from Example 8, Step 1 (0.190 g, 0.700 mmol) in ethanol (3.5 mL) was saturated with ammonia, capped, and heated to 45° C. for three hours. The mixture was cooled, concentrated, and triturated with diethylether. Crude product was recrystallized from dimethylformamide/water to give 0.129 g (77%) of the title compound as a pale yellow solid, one-eighth hydrate: mp 215° C.; 1H NMR (DMSO-d6): δ9.87 (s, 1H), 9.34 (s, 1H), 8.60 (d, 1H), 7.40-8.60 (broad signal, NH2), 8.02 (d, 1H), 7.86 (d, 1H), 7.77 (d, 1H), 7.68 (t, 1H). IR (KBr): 3200, 1800, 1690, 1650 cm-1 ; MS (m/z) 240(MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403854 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-471b585330fd4a03b4b9cedeef057be5 |
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| Source note | uspto-grants-1995_04 |
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