Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | HCID 23729488 | HCID 23729488 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 67076828 | HCID 67076828 | — |
Reaction Steps
N-{[1,6-Diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}-4-({8-[(2-hydroxyethyl)(methyl)amino]octanoyl}amino)benzamide [the “free base”, 100 mg, about 0.161 mmol, as a substantially amorphous form thereof, as prepared in Example 1B (alternative preparation no. 2)] was dissolved in isopropanol (1 ml) at room temperature. Phosphoric acid (H3PO4, 85 wt % solution in water (commercially available e.g. from Aldrich), 3.95 microliters, 0.5 equivalents) was added. A gum formed, which dissolved on heating to 60° C. No precipitation occurred after cooling to ambient temperature and about 30 minutes at ambient temperature. Phosphoric acid (H3PO4, 85 wt % solution in water (commercially available e.g. from Aldrich), 3.95 microliters, 0.5 equivalents) was added. A gum formed, which did not dissolve on heating to 60° C. The reaction mixture was left to temperature cycle between 0° C. and 40° C. for about 2 days. A suspension had formed, and from this the resulting solid was isolated by filtration, washed with isopropanol (0.5 ml) and dried at 40° C. under vacuum overnight. 68.3 mg of dried solid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003663B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d4f6a74064d74c1696b1108eed9818b8 |
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| Source note | uspto-grants-2011_08 |
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