HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 7-bromo-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol | HCID 21094589 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-bromo-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazole | HCID 59702355 | 89% |
Reaction Steps
A solution of 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol (1.75 g, 5.38 mmol), 50 mL of toluene, and 4-toluenesulfonic acid (1.23 g, 6.46 mmol) was stirred at 110° C. for 20 h, then allowed to cool. A saturated aqueous NaHCO3 solution (50 mL) was added, and the mixture was extracted with three 30 mL portions of ethyl acetate. The combined organic layers were dried over MgSO4, filtered, and concentrated to a brown oil. Column chromatography (0→8% EtOAc/hexanes) afforded of 7-bromo-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazole (43; 1.47 g; 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365211B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-fb67c054dff641d6b20006099f1dc5c3 |
| Source note | uspto-grants-2008_04 |