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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946499Generated: October 26, 2026

Trimethylphosphine → Triethyl {3-[(4-chlorophenyl)methyl]-2-cyclopropyl-3,4,5,6-tetrahydrocyclopenta[d]imidazol-4-yl}methanetricarboxylate

https://huagongshe.com/reaction/1946499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylphosphineHCID 68983—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTriethyl methanetricarboxylateHCID 80471—
Reactant3-[(4-Chlorophenyl)methyl]-2-cyclopropyl-3,4,5,6-tetrahydrocyclopenta[d]imidazol-4-olHCID 58460201—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductTriethyl {3-[(4-chlorophenyl)methyl]-2-cyclopropyl-3,4,5,6-tetrahydrocyclopenta[d]imidazol-4-yl}methanetricarboxylateHCID 58460194—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Intermediate 30 (95 mg) and triethylmethanetricarboxylate (0.140 ml) in toluene (1.5 ml) and tetrahydrofuran (1.5 ml), stirred at RT under an inert atmosphere of nitrogen, was added trimethylphosphine, 1M in toluene (0.658 ml). The resulting solution was cooled to −78° C. and diisopropyl azodicarboxylate (0.130 ml) was added dropwise via syringe and the reaction was stirred at −78° C. for 45 mins. The reaction mixture was removed from the cold bath and allowed to warm to RT and stirred under N2 atmosphere overnight. Reaction mixture concentrated in vacuo. The residue was taken up in DCM (20 ml) and washed with water (20 mL). The 2 phases were separated, the organic extract was dried (hydrophobic frit) and concentrated under vacuum. The residue was purified on silica using a cyclohexane:ethyl acetate 0-100% gradient. The desired fractions were combined and concentrated under vacuum to give the title compound (146 mg). LC/MS MH+503, Rt 3.37 min (5 minute run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399444B2
Source datasetuspto-grants-2013_03
ORD IDord-059c371ffae94ed4b77ca596bcd02ca7
Source noteuspto-grants-2013_03