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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427642Generated: November 1, 2026

N,N-Dimethylpropargylamine → HCID 11668403, compound

https://huagongshe.com/reaction/2427642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylpropargylamineHCID 81643—
ReactantHCID 57949704HCID 57949704—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiisopropylamineHCID 7912—
ProductHCID 11668403HCID 1166840362%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-2-(4-phenoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.100 g, 0.25 mmol), PdCl2(PPh3)2 (0.009 g, 0.013 mmol), and CuI (0.0025 g, 0.013 mmol) in diisopropylamine (4 mL) was treated with dimethyl-2-propynyl-amine (0.032 mL, 0.3 mmol). The reaction mixture was stirred at 100° C. for 2 h. After the complete consumption of bromo-isoindolone (monitored using GC-MS), the reaction mixture was cooled to ambient temperature and diluted with ethyl acetate (20 mL). The solids were removed by filtration and the filtrate was concentrated. Silica gel column chromatography of the resulting material using combinations of chloroform-methanol (typically 10:1 CHCl3-MeOH) afforded 5-(3-dimethylamino-prop-1-ynyl)-2-(4-phenoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.061 g, 62%). 1H NMR (300 MHz, CDCl3): δ (ppm) 2.36 (s, 6H), 3.47 (s, 2H), 4.25 (s, 2H), 4.76 (s, 2H), 6.94-7.54 (m, 1H), 7.80 (d, 1H). GC-MS: 396 (M)+, 353 (M−43)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-e5671d1a0b614afa8bfb62a00b8aee0f
Source noteuspto-grants-2011_06