HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270802Generated: October 30, 2026
HCID 21071120, compound → HCID 21071118, compound
https://huagongshe.com/reaction/270802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21071120 | HCID 21071120 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21071118 | HCID 21071118 | — |
Reaction Steps
2.85 g (6.2 mmol) of 2-(5-Azidomethyl-4-chloro-3-trifluoromethyl-pyrazol-1-yl)-1-[4-(4-chlorophenyl)-piperazin-1-yl]-ethanone was dissolved in 80 mL methanol, and 3.61 g (16.0 mmol) of SnCl2 hydrate was added. After two hours, the reaction was concentrated in vacuo to remove the methanol. The residue was partitioned between 0.5M NaOH and ethyl acetate, and the phases were separated. The aqueous phase was back-extracted once with ethyl acetate. The combined ethyl acetate phases were extracted twice with 1M HCl. The acidic aqueous phase was basified with 1M NaOH, and was extracted once with ethyl acetate. The final ethyl acetate phase was washed once with brine, dried over Na2SO4, filtered, and concentrated to an oil. The oil was dissolved in methanol, acidified with 2M HCl in ether, and the product was isolated by filtration after precipitation: 1H NMR (DMSO-d6, 400 MHz) 8.58 (s, 3H), 7.27 (d, 2H), 7.03 (d, 2H), 5.71 (s, 2H), 4.10 (d, 2H), 3.64 (m, 4H), 3.32 (m, 2H), 3.19 (m, 2H) ppm; MS (ES) M+H expected=436.1, found=436.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449576B1 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-1a829ca87a34447c97292e9298778412 |
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| Source note | uspto-grants-2008_11 |
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