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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817704Generated: October 30, 2026

1,4-Cyclohexadiene → HCID 16063180, compound

https://huagongshe.com/reaction/1817704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexadieneHCID 12343—
ReactantHCID 16063048HCID 16063048—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 16063180HCID 16063180—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 2,7-dibenzyl-4-(4-fluoro-phenyl)-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidine hydrochloride in EtOH was added 10% Pd/C (1 equiv) followed by 1,4-cyclohexadiene (5 equiv). The mixture was heated at 85° C. for 5 h, filtered and concentrated. The residue was dissolved in CH2Cl2 and treated with Dowex 550A resin. After 1 h, the resin was removed by filtration and the filtrate was concentrated. Chromatography on SiO2 (2 M NH3 in MeOH/CH2Cl2) afforded the title compound. MS (ESI): exact mass calcd. for C20H18FN3, 319.15; m/z found, 320.4 [M+H]+. 1H NMR (MeOH-d4): 7.70-7.67 (m, 2H), 7.36-7.35 (m, 2H), 7.31-7.25 (m, 4H), 7.20-7.17 (m, 1H), 4.42 (s, 2H), 4.26 (s, 2H), 3.48 (t, J=6.1, 2H), 3.09 (t, J=6.1, 2H). The compounds in Examples 77-81 were prepared using methods similar to those described in Example 76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598255B2
Source datasetuspto-grants-2009_10
ORD IDord-01232a0f327948498c21f86b0c36de1b
Source noteuspto-grants-2009_10