HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → HCID 21109849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 21109851 | HCID 21109851 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21109849 | HCID 21109849 | — |
Reaction Steps
A solution of 0.48 g (1.153 mmol) of 3-{1-[4-(4-cyanophenyl)-1,4-dioxobutyl]-4-piperidinyl}-3,4-dihydro-2(1H)-quinazolinone (Item no. 73) and 1.15 ml of 1N hydrochloric acid in 100 ml of methanol was hydrogenated at ambient temperature under 3 bar of pressure in the presence of 0.25 g of 10% palladium on active charcoal until the uptake of hydrogen had ended. The mixture was freed from catalyst and solvent and yielded 0.27 g (58% of theoretical) of a colourless substance, Rf 0.30 (El A). IR (KBr): 1662.5 (C═O) MS: M+406; ESI: (M+H)+=407
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230001B1 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-090da39771d64a93be486f41114f2d29 |
| Source note | uspto-grants-2007_06 |