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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803847Generated: November 1, 2026

Cyclohexene → HCID 86659259, compound

https://huagongshe.com/reaction/1803847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantHCID 86659258HCID 86659258—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86659259HCID 8665925995%

Reaction Steps

5-Benzyloxy-3-{4-(4-methyl-piperazin-1-yl)-2-[(tetrahydro-pyran-4-yl)-(2,2,2-trifluoro-acetyl)-amino]-benzoylamino}-indazole-1-carboxylic acid tert-butyl ester (2.3 g, 3.13 mmol) in dioxane (46 mL) was treated with cyclohexene (18 mL) and 10% Pd/C (1.6 g). The mixture was stirred at reflux temperature. After 1.5 hs it was filtered over a celite funnel and washed with dioxane. Evaporation of the solvent left a solid that was washed with Et2O. After drying at 45° C. under vacuum, 1.92 g of title compound in 95% yield were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354399B2
Source datasetuspto-grants-2013_01
ORD IDord-d6643b0518634840b42335d78ed02c00
Source noteuspto-grants-2013_01