Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 25095385 | HCID 25095385 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25095386 | HCID 25095386 | — |
Reaction Steps
Initially charge 137 mg (0.285 mmol) of 3-(4-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]-pyrimidin-4-yl]oxy}phenyl)propanoic acid methyl ester in 4.5 ml of THF, and add 0.855 ml of 1N sodium hydroxide solution at RT. Stir the mixture at 50° C. for 1 h. After cooling, acidify with 1N hydrochloric acid and filter off the precipitated solid with suction, wash with water and dry under high vacuum. 125.9 mg (94.7% of theory) of the target compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324222B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-acd466d9634342de80e344a3d65989ee |
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| Source note | uspto-grants-2012_12 |
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