HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylamine → HCID 10983514, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-Allyl-2,2,2-trifluoroacetamide | HCID 558569 | — |
| Reactant | HCID 11016069 | HCID 11016069 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10983514 | HCID 10983514 | 60% |
Reaction Steps
(Method P) Under an atmosphere of nitrogen, trifluoromethanesulphonic acid 3-chloro-8-methyl-8H-quino[4,3,2-kl]acridin-6-yl ester, 38 (30 mg, 0.075 mmol), allyltrifluoroacetamide (17 mg, 1.5 eq), palladium (II) acetate (2 mg, 10 mol %), triphenyl phosphine (4 mg, 20 mol %), dicyclohexylamine (0.032 mL, 2 eq), and dioxane were mixed in a sealed tube and heated reflux in a sealed tube for 18 hrs. On cooling, the products were dissolved in dichloromethane and adsorbed onto silica. Separation of the more polar product by column chromatography (85:15 hexane:ethyl acetate) gave the title compound (22 mg, 0.045 mmol, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115619B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-7b1571f8a04047819d458c7d63e9b71d |
| Source note | uspto-grants-2006_10 |