Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 25058137 | HCID 25058137 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67000936 | HCID 67000936 | — |
Reaction Steps
step 1—A suspension of 3-[6-bromo-2-fluoro-3-(1H-pyrazolo[3,4-c]pyridazin-3-ylmethyl)-phenoxy]-5-chloro-benzonitrile (R-73, 1.32 g, 2.88 mmol), 37% aqueous formaldehyde (100 mL) and MeOH (100 mL) was stirred at 67° C. for 35 h. The volatile solvents were evaporated and the residue diluted with H2O and the resulting precipitate filtered, washed with H2O and air-dried to afford 1.27 g of 3-[6-bromo-2-fluoro-3-(1-hydroxymethyl-1H-pyrazolo[3,4-c]pyridazin-3-ylmethyl)-phenoxy]-5-chloro-benzonitrile (12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063028B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-1b54e2d7fe514c2d8250e331e815982c |
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| Source note | uspto-grants-2011_11 |
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