HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 9971204, compound → HCID 131719632, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 9971204 | HCID 9971204 | — |
| Reactant | HCID 19047580 | HCID 19047580 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131719632 | HCID 131719632 | — |
Reaction Steps
A reaction mixture containing thiazolo[3,2-b]isoquinolinium perchlorate (2.4 g; 8.4 mmol) and 1,1-di-[(1-p-methoxybenzyl)-pyrazol-3-yl)ethylene (4 g; 0.01 mol) in 125 ml of ethanol and 25 ml of acetonitrile was refluxed for 12 h under nitrogen. The reaction mixture was cooled to room temperature, the solid product was filtered, washed with ether, and dried in vacuo to afford 4.65 g (81.6%) of 11,11-di-[(1-p-methoxybenzyl)-pyrazol-3-yl)]-5,10-ethano-5,10-dihydrothiazolo[3,2-b]isoquinolinium perchlorate (Formula I: A=thiazolo; R1 =R2 =R3 =R6 =H; R4 =R5 =1-p-methoxybenzyl-3-pyrazolyl; X- =ClO4-).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05604224 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-7b319385d10c48c9a9d542f885325646 |
| Source note | uspto-grants-1997_02 |