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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491520Generated: October 26, 2026

Sodium Iodide → HCID 19422762, compound

https://huagongshe.com/reaction/1491520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCarbonic acid, 1-chloroethyl ethyl esterHCID 162095—
Reactantpotassium 5-(N-acetylamino)-3-(methylaminocarbonyl)-2,4,6-triiodobenzenecarboxylateHCID 23692363—
SolventDimethylformamideHCID 6228—
ProductHCID 19422762HCID 19422762—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Chloroethyl ethyl carbonate (1.67 g, 11.0 mmol) was added dropwise at room temperature to a solution of potassium 5-(N-acetylamino) -3-(N-methylaminocarbonyl)-2,4,6-triiodobenzenecarboxylate (6.52 g, 10.0 retool) and sodium iodide (150 rag, 1.0 retool) in dry DMF (50 ml). After stirring at 50° C. for 24 hours the solvent was removed at reduced pressure. The residue was dissolved in chloroform and washed four times with a saturated sodium hydrogen carbonate solution and twice with water. After drying with magnesium sulfate and filtration, the solvent was removed at reduced pressure to give the title compound. Yield: (2.2 g, 38 %). Purity by HPLC: 98%. 1H-NMR (DMSO (DMSO-6 ): delta=1.24 (t, J=7 Hz, CH3); 1.63 (d, J=6 Hz, CH3); 2.03 (s, CH3CO); 2.75 (d, J=3 Hz, NCH3); 4.21 (q, J=7 Hz, CH2): 6.93 (q, J=6 Hz, CH); 8.4-8.7 (m, NHMe); 10.03 ppm (s, NHAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05370861
Source datasetuspto-grants-1994_12
ORD IDord-321846efb8774f5786c9b484c58c957b
Source noteuspto-grants-1994_12