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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588088Generated: October 31, 2026

N-bromobutanimide → 4-(bromomethyl)-6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/588088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-chloro-3-methoxy-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118272149—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product4-(bromomethyl)-6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118271789—

Reaction Conditions

Temperature70 °C

Reaction Steps

6-Chloro-3-methoxy-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridine (1.5 g, 3.41 mmol) was dissolved in CCl4 (10 mL), charged with NBS (637 mg, 3.58 mmol) and AlBN (56.0 mg, 0.341 mmol), and heated to 70° C. overnight. The reaction was diluted with DCM (10 mL) and purified by flash chromatography (5-25% EtOAc/hexanes) to give 4-(bromomethyl)-6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridine. MS ESI calc'd. for C27H21BrClN3O [M+1]+519. found 519.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226922B2
Source datasetuspto-grants-2016_01
ORD IDord-df5050c4d9134430a27d1efe6361b819
Source noteuspto-grants-2016_01