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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044027Generated: October 31, 2026

Trityl chloride → 3-(4-Bromothiazol-2-yl)-1-trityl-pyrazolo[5,4-b]pyridine

https://huagongshe.com/reaction/1044027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178419473HCID 178419473—
SolventDimethylformamideHCID 6228—
Product3-(4-Bromothiazol-2-yl)-1-trityl-pyrazolo[5,4-b]pyridineHCID 68107919—

Reaction Steps

A solution of 3-(4-bromothiazol-2-yl)-1H-pyrazolo[5,4-b]pyridine (161 mg, 0.5727 mmol) in DMF (3 mL) was cooled to 0° C. then sodium hydride (27.49 mg, 0.6872 mmol) was added in one portion. Stirred at 0° C. for 30 mins before (chloro-diphenyl-methyl)benzene (167.6 mg, 0.6013 mmol) was added. Ice-bath removed and stirred at room temperature for 2 h. Quenched with water, diluted with EtOAc. Organic layer then collected, washed with brine, dried (MgSO4), filtered and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563576B2
Source datasetuspto-grants-2013_10
ORD IDord-bb4000145e464270b80dd48d9fe43aab
Source noteuspto-grants-2013_10