Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178492083 | HCID 178492083 | — |
| Solvent | Methanesulfonic Acid | HCID 6395 | — |
| Product | HCID 178515076 | HCID 178515076 | 76% |
Reaction Steps
7-Chloro-2-(3-chloro-4-methoxyphenyl)-4-hydroxy-1,2,5,10-tetrahydropyridazino[4,5-b]quinoline-1,10-dione (previously prepared in Example 37 1.00 g, 2.47 mM) was stirred in methanesulfonic acid (20 mL) to give a black solution. This solution was heated to 145° C. for 6 hours and cooled to room temperature. Water (60 mL) was added to give a tan suspension which was stirred for 3 hours and filtered. The collected solids were washed with water and ether to give the title compound as a gold powder (0.98 g, 76 %), mp 350-353° C.; MS(CI): 390.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214826B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-cfa01be6ce344e3681fcd51f069e7400 |
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| Source note | uspto-grants-2001_04 |
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