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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571411Generated: November 2, 2026

tert-Butyl hydroperoxide → HCID 178506289, compound

https://huagongshe.com/reaction/571411

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium trifluoromethanesulfinateHCID 23690734—
Reactant6-Chloro-1H-pyrazolo(4,3-c)pyridineHCID 56932109—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178506289HCID 178506289—

Reaction Steps

Ref: PCT Int. Appl., 2010086251, 2010. To a suspension of 6-chloro-1H-pyrazolo[4,3-c]pyridine (1a, 1 g, 6.51 mmol), sodium trifluoromethanesulfinate (3.05 g, 19.54 mmol) in 10 mL of DCM and 4 mL of H2O, 70% tert-butyl hydroperoxide (4.19 g, 32.6 mmol) aqueous solution was added. The heterogeneous reaction mixture was stirred vigorously at r.t. After 28 hr, LCMS analysis showed partial conversion. Additional sodium trifluoromethanesulfinate (3.05 g, 19.54 mmol) and tert-butyl hydroperoxide (4.19 g, 32.6 mmol) was added and the reaction mixture was stirred over the weekend. Water, DCM and aqueous Na2S2O3 was added. A yellow solid was filtered off and the filtrate was extracted with DCM. The organic layer was concentrated and purified (50 g silica gel, eluting with 1:30 MeOH/DCM) to give 6-chloro-3-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridine as a yellow solid, which was further purified by recrystallization from MeOH/DCM/Hexane (200 mg, 13%). MS ESI calc'd. for C7H3ClF3N3[M+1]+ 222, found 222.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023865B2
Source datasetuspto-grants-2015_05
ORD IDord-4be1d5aafdcf4d63b304f4eea0b174c8
Source noteuspto-grants-2015_05