HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497669Generated: October 25, 2026
Heptafluorobutyryl Chloride → N-[6-chloro-1H-indazol-3-yl]-2,2,3,3,4,4,4-heptafluorobutanamide
https://huagongshe.com/reaction/497669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptafluorobutyryl Chloride | HCID 67810 | — |
| Reactant | 6-chloro-1H-indazol-3-amine | HCID 85628 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[6-chloro-1H-indazol-3-yl]-2,2,3,3,4,4,4-heptafluorobutanamide | HCID 22319502 | — |
Reaction Steps
0.60 cm3 of heptafluorobutyryl chloride is added to 1 g of 6-chloro-1H-indazole-3-amine in 10 cm3 of pyridine, after cooling the medium to about 6° C., the mixture is then allowed to return to room temperature over 19 hours and is evaporated to dryness under reduced pressure (2 kPa; 45° C.). The residue is taken up in 40 cm3 of ethyl acetate and 20 cm3 of water; the precipitate formed is filtered off on a sinter funnel and then rinsed with 2×10 cm3 of methylene chloride and purified by chromatography under an argon pressure of 50 kPa, on a column of silica gel (particle size 40-60 μm; diameter 3.5 cm), eluting with a cyclohexane/ethyl acetate mixture (70/30 by volume). The fractions containing the expected product are combined and evaporated under reduced pressure (2 kPa; 50° C.) to give 0.77 g of N-[6-chloro-1H-indazol-3-yl]-2,2,3,3,4,4,4-heptafluorobutanamide in cottony form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949579B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-de4280bf980547e79b0f3ae124c4f49f |
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| Source note | uspto-grants-2005_09 |
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