HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588157Generated: October 30, 2026
2,2-Difluoro-2-(fluorosulfonyl)acetic acid → HCID 118272222, compound
https://huagongshe.com/reaction/588157
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-Difluoro-2-(fluorosulfonyl)acetic acid | HCID 2737516 | — |
| Reactant | HCID 118272021 | HCID 118272021 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118272222 | HCID 118272222 | 55.5% |
Reaction Steps
A mixture of 2-((6-chloro-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-yl)oxy)ethanol (58B, 500 mg, 0.987 mmol) and copper(I) iodide (282 mg, 1.480 mmol) in acetonitrile (2861 μl) were degassed (evacuated and back filled w/Argon). 2,2-difluoro-2-(fluorosulfonyl)acetic acid (153 μl, 1.480 mmol) was added, degassed, and heated at 80° C. for 30 min. Reaction was quenched with water (1 mL), diluted with EtOAc and filtered through a celite pug. The solution was concentrated in vacuo on silica. Material was purified by normal phase column chromotography eluting with Hex/EtOAc (0-20%) affording 6-chloro-3-(2-(difluoromethoxy)ethoxy)-1-trityl-1H-pyrazolo[4,3-c]pyridine (59B, 277 mg, 0.547 mmol, 55.5% yield) as a white crystalline solid. MS: [M+H]+ m/z 506.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226922B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-1b97f2c474314548aee83dfa05c6f91b |
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| Source note | uspto-grants-2016_01 |
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