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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911736Generated: November 1, 2026

Cyclohexylamine → HCID 66707052, compound

https://huagongshe.com/reaction/911736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86629659HCID 86629659—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 66707052HCID 6670705233.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

Slurry palladium(II) acetate (434 mg, 1.9 mmol), BINAP (1.2 g, 1.9 mmol), sodium-tert-butoxide (644 mg, 6.7 mmol), cyclohexylamine (1.4 g, 14.4 mmol) and 3-tert-butoxycarbonyl-7-chloro-6-(6-chloro-pyridin-3-ylmethylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (2.1 g, 4.8 mmol) in anhydrous toluene (70 mL). Degas the slurry under house vacuum, then buble nitrogen. Heat the mixture to 95° C. for 16 h under a nitrogen atmosphere. Cool the mixture to room temperature, dilute with EtOAc (50 mL) and filter through Celite®. Concentrate the filtrate to an oil and purify by chromatography on silica gel eluting with hexane/EtOAc (19:1 to 13:7 gradient) to obtain 3-tert-butoxycarbonyl-7-chloro-6-(6-cyclohexylamino-pyridin-3-ylmethylthio)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (800 mg, 33%). MS (ES+) m/z: 502.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-93b06e88b498484280ff92c2b6de132a
Source noteuspto-grants-2011_09