HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902539Generated: October 26, 2026
Potassium Phosphate, Tribasic → 2,3-dimethyl-7-(2,4,6-trimethyl-phenyl)-2H-indazole
https://huagongshe.com/reaction/902539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2,4,6-Trimethylbenzeneboronic acid | HCID 292184 | — |
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | 7-Bromo-2,3-dimethyl-2H-indazole | HCID 44119473 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 2,3-dimethyl-7-(2,4,6-trimethyl-phenyl)-2H-indazole | HCID 58861008 | — |
Reaction Steps
A flask containing 7-bromo-2,3-dimethyl-2H-indazole (3.23 g, 14.4 mmol), 2,4,6-trimethylphenyl boronic acid (3.51 g, 21.4 mmol), freshly ground potassium phosphate (6.04 g, 28.5 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.225 g, 0.572 mmol), and palladium(II) acetate (0.032 g, 0.14 mmol) was evacuated and back-filled with nitrogen. Toluene (50 mL) was added, and the yellow-orange mixture was stirred at 100° C. for 22 h then allowed to cool. Ether (200 mL) was added, and the yellow solution was decanted from a dark granular solid. The organic layer was sequentially washed with 200 mL of a 10% aqueous NaOH solution and 200 mL of a saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated to a pale yellow solid. Column chromatography (0→33% EtOAc/hexanes) afforded 2,3-dimethyl-7-(2,4,6-trimethyl-phenyl)-2H-indazole as an off-white solid (7: R=R′=Me, Ar=2,4,6-trimethylphenyl; 3.03 g, 79%; m.p. 162-164).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365211B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-c44bf591ad4445368af7fa648eed8a54 |
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| Source note | uspto-grants-2008_04 |
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