HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183830Generated: November 3, 2026
HCID 68379942, compound → HCID 69926609, compound
https://huagongshe.com/reaction/1183830
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 68379942 | HCID 68379942 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69926609 | HCID 69926609 | — |
Reaction Steps
To a solution of 3-[(1S,2S)-2-hydroxycyclohexyl]-6-[4-(1-hydroxyprop-2-en-1-yl)benzyl]pyrido[3,4-h]quinazolin-4(3H)-one (0.010 g, 0.023 mmol) in 3 mL of methanol was added palladium on carbon (4.0 mg, 0.037 mmol). The mixture was placed under an atmosphere of hydrogen (1 atm) for 4 h and was then filtered through a pad of Celite, which was washed with MeOH. The filtrate was concentrated in vacuo to provide the title compound that gave a proton NMR spectra consistent with theory and a mass ion (ES+) of 443.9 [M+H]+: 1H NMR (400 MHz, CDCl3 δ 9.37 (s, 1H), 8.63 (s, 1H), 8.56 (s, 1H), 8.26 (s, 1H), 8.08 (s, 1H), 7.26-6.88 (m, 4H), 4.65-4.45 (m, 3H), 4.07 (br s, 1H), 3.66-3.37 (m, 3H), 2.84 (br s, 1H), 2.31-2.23 (m, 1H), 2.07-1.67 (m, 5H), 1.40-0.86 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08664387B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-cf0b5dbcad674613bf722ec2c3dc4df7 |
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| Source note | uspto-grants-2014_03 |
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