HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508198Generated: October 30, 2026
2,6-Dichlorobenzoyl chloride → HCID 68159440, compound
https://huagongshe.com/reaction/508198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorobenzoyl chloride | HCID 78392 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 68159279 | HCID 68159279 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68159440 | HCID 68159440 | — |
Reaction Steps
To a solution of a mixture of regio-isomers of 3-(4-(1-(4-Methoxybenzyl)-1H-tetrazol-5-yl)phenyl)-1H-indazole (Example 20, step i) (50 mg, 0.13 mmol) was dissolved in anhydrous THF (1 ml). After addition of t-BuOK (16 mg, 0.14 mmol,) the reaction mixture was stirred at room temperature for 15 min. Subsequently, 2,6-dichlorobenzoyl chloride (21 μl, 0.14 mmol) was added and the reaction mixture was stirred for another 2 h at room temperature. The solvent was evaporated under reduced pressure, the residue was dissolved in dichloromethane and washed with water, an aqueous solution of 5% K2CO3 and water. The organic solvent was evaporated under reduced pressure and the residue was dried in vacuo. The product was purified by preparative HPLC to afford (2,6-dichlorophenyl)(3-(4-(1-(4-methoxybenzyl)-1H-tetrazol-5-yl)phenyl)-1H-indazol-1-yl)methanone as a mixture of 2 regioisomers in a 98 to 2 ratio (59 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09095583B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-1bc1d943f81b4fe88c53c2be6d76a2ea |
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| Source note | uspto-grants-2015_08 |
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