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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407914Generated: October 30, 2026

1,2-Diaminocyclohexane, trans- → HCID 67469775, compound

https://huagongshe.com/reaction/407914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantSodium methanesulfinateHCID 2733271—
ReactantHCID 67469699HCID 67469699—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 67469775HCID 6746977553.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

Tert-butyl 4-((3S,4S)-4-(benzyloxy)-3-(4-bromo-2-fluorophenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (300 mg, 0.532 mmol) was dissolved in DMSO (5 mL) and degassed for 10 minutes. Sodium methanesulfinate (81.5 mg, 0.799 mmol) and trans-cyclohexane-1,2-diamine (25.6 μL, 0.213 mmol) were added, followed by Cu(I) triflate benzene complex (26.8 mg, 0.0532 mmol) and the reaction was heated to 110° C. overnight. The reaction was cooled, partitioned between water and EtOAc, extracted with EtOAc, washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified over silica gel (100% EtOAc) to afford tert-butyl 4-((3S,4S)-4-(benzyloxy)-3-(2-fluoro-4-(methylsulfonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (160 mg, 0.284 mmol, 53.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-7194b2a508cc46cfbdfc98443af2e881
Source noteuspto-grants-2014_06