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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707548Generated: October 30, 2026

Sodium Iodide → (2-Thienylcarbonyloxy)methyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate

https://huagongshe.com/reaction/1707548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChloromethyl Thiophene-2-carboxylateHCID 11148043—
Reactantcesium 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23675689—
SolventDimethylformamideHCID 6228—
Product(2-Thienylcarbonyloxy)methyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 18961595—

Reaction Steps

Chloromethyl 2-thiopbenecarboxylate (0.63 g, 3.6 mmol) (Intermediate 6) in dry DMF (70 ml) is added dropwise at 50° C. to a solution of cesium 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate (3.00 g, 3.9 mmol) and sodium iodide (28 mg, 0.19 mmol) in dry DMF (45 ml). The precipitate is removed by filtration after stirring for 4 hours and the solvent is removed at reduced pressure. The residue is dissolved in chloroform (50 ml) and washed four times with a saturated sodium hydrogen carbonate solution. After drying with magnesium sulfate the solvent is removed at reduced pressure to give the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354549
Source datasetuspto-grants-1994_10
ORD IDord-99a08d8eedec450ba4db09fa18f40e82
Source noteuspto-grants-1994_10