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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68159279HCID 68159279—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68159440HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095583B2
Source datasetuspto-grants-2015_08
ORD IDord-1bc1d943f81b4fe88c53c2be6d76a2ea
Source noteuspto-grants-2015_08