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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091688Generated: November 2, 2026

Iodine → HCID 178430462, compound

https://huagongshe.com/reaction/2091688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactanttert-ButanolHCID 6386—
ReactantPropylenediamineHCID 6567—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86640156HCID 86640156—
ProductHCID 178430462HCID 17843046232%

Reaction Steps

To 4-(2,4-dichlorophenyl)-5-formyl-2-morpholin-4-ylthiophene-3-carbonitrile (52.0 mg, 0.000142 mol) in tert-butyl alcohol (0.75 g, 0.010 mol) was added 1,2-diaminopropane (12.9 mg, 0.000174 mol) and the mixture was stirred for 30 min. Iodine (51 mg, 0.00020 mol) and potassium carbonate (65.7 mg, 0.000475 mol) was added the mixture was stirred at 70° C. for 3 hr. The reaction mixture was quenched by saturated sodium bicarbonate solution and brine. The organic layer was collected and purified by column chromatography to afford 4-(2,4-dichlorophenyl)-5-(4-methyl-4,5-dihydro-1H-imidazol-2-yl)-2-morpholinothiophene-3-carbonitrile (19 mg, 32%). LCMS: (FA) ES+ 421. 1H NMR (400 MHz, d1-chloroform) δ: 7.60 (s, 1H), 7.50-7.40 (m, 1H), 7.40-7.30 (m, 1H), 4.20-4.05 (m, 1H), 3.90-3.75 (m, 5H), 3.60-3.70 (m, 4H), 3.38-3.20 (m, 1H), 1.25 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440664B2
Source datasetuspto-grants-2013_05
ORD IDord-5385df8004774ed7919492a4f62e1244
Source noteuspto-grants-2013_05