HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (+)-3,4-dihydro-5-methyl-2-[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]pyrimido[1,6-a]indol-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-methyl-2-[2-[[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]amino]ethyl]indole | HCID 10029785 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (+)-3,4-dihydro-5-methyl-2-[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]pyrimido[1,6-a]indol-1(2H)-one | HCID 10460239 | — |
Reaction Steps
A mixture of (-)-3-methyl-2-[2-[[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]amino]ethyl]indole (2.7 g), N,N'-carbonyldiimidazole (2.2 g), 1,8-diazabicyclo[5.4.0]-7-undecene (861 mg) and molecular sieves (810 mg) in dry tetrahydrofuran (40 ml) was stirred at reflux for 2 hours. The reaction mixture was diluted with ethyl acetate, washed with water and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was chromatographed over silica gel (eluted with 5% ethyl acetate in chloroform) to give (+)-3,4-dihydro-5-methyl-2-[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]pyrimido[1,6-a]indol-1(2H)-one (2.09 g) as amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05256780 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-1bae87ad33de4776aaf14ff0bb91ce87 |
| Source note | uspto-grants-1993_10 |