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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441289Generated: November 1, 2026

Acetic Acid → HCID 178487433, compound

https://huagongshe.com/reaction/1441289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(6-Methoxy-4-phenylpyridazin-3-yl)benzaldehydeHCID 59164359—
ReactantHCID 178420066HCID 178420066—
SolventDimethylformamideHCID 6228—
ProductHCID 178487433HCID 178487433—

Reaction Steps

4-(6-Methoxy-4-phenylpyridazin-3-yl)benzaldehyde (2-2; 80 mg, 0.27 mmol) was dissolved in dry dimethylformamide (2 mL) and 2-(3-piperidin-4-yl-1H-pyazol-5-yl)pyridine (1-4; 99 mg, 0.43 mmol) and acetic acid (0.14 mL, 2.3 mmol) were added. After stirring for 15 min., sodium triacetoxyborohydride (116 mg, 0.54 mmol) was added and the reaction mixture was stirred at ambient temperature for 12 hours. This reaction mixture was partially evaporated and the residue chromatographed on a silica gel column eluting with a 0-5% methanol/ethyl acetate sat'd with NH4OH. 3-methoxy-5-phenyl-6-(4-{[4-(5-pyridin-2-yl-1H-pyrazol-3-yl)piperidin-1-yl]methyl}phenyl)pyridazine (2-3) was obtained as a nearly pure viscous oil. NMR (CDCl3): δ8.60 (1H, d, J=5 Hz), 7.69-7.72 (2H, m), 7.23-7.35 (6H, m), 7.17 (2H, br d, J=7 Hz), 6.98 (1H, s), 6.61 (1H, s), 4.22 (3H, s), 3.52 (2H, s), 2.95 (2H, d, J=12 Hz), 2.72 (1H, m), 2.10 (2H, br t, J=1 Hz), 1.97 (2H, br d, J=12 Hz), 1.81 (2H, br q, J=11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655649B2
Source datasetuspto-grants-2010_02
ORD IDord-41f5dea5f2e341be991aade1b4c01063
Source noteuspto-grants-2010_02