Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 71008253 | HCID 71008253 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 71008224 | HCID 71008224 | 95% |
Reaction Steps
In a 25 mL round-bottomed flask, 1-(3-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-2-(hydroxymethyl)phenyl)-6-(2-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile (4 mg, 6.92 μmol) and [hydrogen bis(dimethylphosphinito-kP)]platinum (II) (29.7 μg, 0.0692 μmol, Eq: 0.01) were combined with Ethanol (853 μl) and Water (853 μl) to give a colorless solution. The reaction mixture was heated to 45° C. and stirred for 1 h, then concentrated in vacuo. Mixture was diluted with acetonitrile and water and filtered. The resultant filtrate is lyophalized to give 1-[3-(6-tert-Butyl-8-fluoro-1-oxo-1H-phthalazin-2-yl)-2-hydroxymethyl-phenyl]-6-(2-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid amide (3.9 mg, 95%, [M+H]+ 596).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729078B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-52f632a330644601a7f2aeb5aac728bd |
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| Source note | uspto-grants-2014_05 |
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