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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558074Generated: October 30, 2026

Formaldehyde → HCID 67000936, compound

https://huagongshe.com/reaction/558074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantHCID 25058137HCID 25058137—
SolventMethanolHCID 887—
ProductHCID 67000936HCID 67000936—

Reaction Conditions

Temperature67 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063028B2
Source datasetuspto-grants-2011_11
ORD IDord-1b54e2d7fe514c2d8250e331e815982c
Source noteuspto-grants-2011_11