HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571411Generated: November 2, 2026
tert-Butyl hydroperoxide → HCID 178506289, compound
https://huagongshe.com/reaction/571411
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium trifluoromethanesulfinate | HCID 23690734 | — |
| Reactant | 6-Chloro-1H-pyrazolo(4,3-c)pyridine | HCID 56932109 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178506289 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023865B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-4be1d5aafdcf4d63b304f4eea0b174c8 |
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| Source note | uspto-grants-2015_05 |
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