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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224204Generated: November 1, 2026

Triphenylphosphine → HCID 11990202, compound

https://huagongshe.com/reaction/2224204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant[1-(Pyrimidin-2-yl)piperidin-4-yl]methanolHCID 2776521—
Reactant7,8-bis(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-oneHCID 11164161—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11990202HCID 1199020242%

Reaction Steps

The title compound was prepared using 7,8-bis(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one, (50 mg, 0.14 mmol), prepared as described in Example 1, Ph3P (110 mg, 0.42 mmol) and (1-(pyrimidin-2-yl)piperdin-4-yl-)methanol (28 mg, 0.14 mmol) in THF (1.0 mL) and by following the procedure described in Example 2. The title compound, 7,8-bis(4-chlorophenyl)-2-((1-(pyrimidin-2-yl)piperidin-4-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one, (31 mg, 42%) was obtained as yellow powder. MS M+H=532; 1H NMR (CDCl3) δ 8.28 (2H, d, J=5.0 Hz), 8.16 (1H, s), 7.28-7.36 (6H, m), 7.11 (2H, d, J=10.0 Hz), 6.44 (1H, t, J=5.0 Hz), 4.75 (2H, d, J=15.0 Hz), 3.96 (2H, d, J=10.0 Hz), 2.85 (2H, m), 2.20-2.30 (1H, m), 1.74 (2H, d, J=10.0 Hz), 1.30-1.40 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-dd252d856b3a4118b1b46cd88ca1726b
Source noteuspto-grants-2008_05