Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 68424803 | HCID 68424803 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68425488 | HCID 68425488 | — |
Reaction Steps
To a solution of compound 26.1 (0.72 mmol) in THF (5.0 mL) was added aqueous 1.0 M LiOH (6.0 equivalents). The reaction mixture was stirred at 70° C. until all of the starting material was consumed. The reaction was cooled, neutralized with 10% HCl and concentrated to dryness under reduced pressure to provide 4-{2-[4-(3-trifluoromethyl-benzoylamino)-phenyl]-ethylamino}-thieno[3,2-d]pyrimidine-6-carboxylic acid (compound 26.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601725B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-a93ba8913c7848eaaf91e8fe5b9c5286 |
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| Source note | uspto-grants-2009_10 |
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