Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 14075007 | HCID 14075007 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14075008 | HCID 14075008 | 50% |
Reaction Steps
0.90 g (2.12 mmoles) of 9-(4-acetyl-3-hydroxy-2-n-propylphenoxymethyl)-4-oxo-pyrido[1,2-a]pyrimidine-3carboxylic acid ethyl ester and 8 ml of 6N hydrochloric acid were added to 36 ml of acetic acid, and this mixture was heated at 80° C. for 8 hours with stirring. After cooling, the resulting reaction solution was concentrated under reduced pressure, followed by the addition of an appropriate amount of water. The solid matter which separated out was collected by filtration and washed with water. This precipitate was dried and then recrystallized from a mixture of tetrahydrofuran and methanol to obtain 0.42 g (50% yield) of 9-(4-acetyl-3-hydroxy-2-n-propylphenoxymethyl)-4-oxo-pyrido[1,2-a]-pyrimidine-3-carboxylic acid in the form of white crystals. These crystals had a melting point of 170°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04798832 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-930b8a41ffe94e7b8316de162b510be9 |
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| Source note | uspto-grants-1989_01 |
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