Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178490932 | HCID 178490932 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 178509958 | HCID 178509958 | — |
Reaction Steps
3-chloro-5-[2-chloro-5-({6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridin-3-yl}methoxy)phenoxy]benzonitrile (37-8) was dissolved in 6 mL of TFA and heated to 60° C. for 7 hours until reaction was complete as determined by LC/MS analysis. After removal of all volatile material the crude residue was purified via prep HPLC (20%-70% acetonitrile in H2O: C18 Phenomenex Gemini) and lyophilzed from dioxane to yield the title compound in the form of a TFA salt. H1 NMR (CD3OD): 5.40 (s 2H), 6.58 (d, 1H), 6.96 (d, 1H), 7.04 (d, 1H), 7.16 (s, 1H), 7.18 (s, 1H), 7.58 (d, 1H), 7.52 (s, 1H), 8.10 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807684B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-43d984bd8fa543158c2e68799370c7ae |
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| Source note | uspto-grants-2010_10 |
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