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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192984Generated: November 1, 2026

Diisopropylamine → HCID 59375684, compound

https://huagongshe.com/reaction/2192984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantCyclopropylacetyleneHCID 138823—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
ReactantHCID 59375664HCID 59375664—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthyl AcetateHCID 8857—
ProductHCID 59375684HCID 59375684—

Reaction Conditions

Temperature45 °C

Reaction Steps

9-bromo-4-iodo-6-[(1,2,2-trimethylpropyl)amino]benzo[c]-1,6-naphthyridin-1(2H)-one (5.03 g, 10.06 mmol), copper(I) iodide (0.230 g, 1.207 mmol), Pd(allyl)Cl dimer (0.221 g, 0.603 mmol) and tri(2-furyl)phosphine (0.280 g, 1.207 mmol) were combined in a 10-dram vial that was then flushed with nitrogen and kept under a nitrogen atmosphere. MeCN (101 ml) was then added followed by diisopropylamine (4.30 ml, 30.2 mmol) and cyclopropylacetylene (2.57 ml, 30.2 mmol). The resulting solution was then heated to 45° C. and stirred in the dark for 30 min. Then, the reaction was poured into ethyl acetate (350 mL) and washed with sat NaHCO3, water, brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting oil was purified by column chromatography on silica gel, eluting with EtOAc/Hexanes to afford the title compound as a pale yellow solid. LRMS (ESI) calc'd for (C23H25BrN3O) [M+H]+, 438.1; found 438.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329722B2
Source datasetuspto-grants-2012_12
ORD IDord-44864404b8a64defaef748c6a66ee5cc
Source noteuspto-grants-2012_12