Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 90052380 | HCID 90052380 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117856534 | HCID 117856534 | 64.1% |
Reaction Steps
To (S,E)-ethyl 6-((5-(5-(2-(4-(dimethylamino)-N-methyl-2-butenamido)propaneamido)-1-pentyn-1-yl)-4-(propylamino)pyrimidin-2-yl)amino)-1H-indazole-1-carboxylate (21-23, 17.3 mg), tetrahydrofuran (1.0 mL) and 1.0 mol/L aqueous lithium hydroxide (1.0 mL) were added at room temperature, and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture, water and ethyl acetate were added. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (eluent, 100 to 90% ethyl acetate in methanol) to obtain (S,E)-N-(1-((5-(2 -((1H-indazol-6-yl)amino)-4-(propylamino)pyrimidin-5-yl)-4-pentyn-1-yl)amino)-1-oxopropan-2-yl)-4-(dimethylamino)-N-methyl-2-butenamide (21-53, 9.8 mg) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145415B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-9e5e3cc8fb1340d9bc6ee297b8fb58a6 |
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| Source note | uspto-grants-2015_09 |
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