Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 25095387 | HCID 25095387 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25095388 | HCID 25095388 | — |
Reaction Steps
Initially charge 1000 mg (2.085 mmol) of 3-(3-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]-pyrimidin-4-yl]amino}phenyl)propanoic acid methyl ester in 30 ml of THF and add 6.3 ml of 1N sodium hydroxide solution at RT. Stir the mixture at 50° C. for 1 h and then, after cooling, acidify slightly with 1N hydrochloric acid. Filter off the precipitated solid with suction, wash repeatedly with water and dry at 40° C. under high vacuum overnight. 934.5 mg (96.3% of theory) of the target product are obtained as a colourless solid.
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-294acbaf20d44929b981fc026618b4a7 |
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| Source note | uspto-grants-2012_12 |
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