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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617630Generated: October 31, 2026

Thionyl Chloride → 3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole

https://huagongshe.com/reaction/617630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole-3-methanolHCID 15428638—
ReactantChloroform ethanolHCID 21889567—
SolventDichloromethaneHCID 6344—
Product3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazoleHCID 15428639—

Reaction Steps

5,6-Dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole-3-methanol (180.0 g) was ground into a powder form using a mortar and suspended in dichloromethane (1,700 ml) at room temperature. After suspension, the reaction solution was stirred with cooling in an ice bath. To this was added dropwise 48.6 ml of thionyl chloride spending 5 minutes. It was observed 1 minute thereafter that the spot of the material almost disappeared on a thin layer chromatography (chloroform/ethanol=30/1). The reaction solution was poured into saturated sodium bicarbonate aqueous solution (2,000 ml) and extracted with chloroform (5,000 ml), and the extract was dried with sodium sulfate, filtered and then evaporated under a reduced pressure to obtain colorless solid (165.1 g). This solid substance was used in the subsequent reaction as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948913
Source datasetuspto-grants-1999_09
ORD IDord-01fda1a5764a4ddc9b03174ac6869a51
Source noteuspto-grants-1999_09