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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233060Generated: October 31, 2026

Pyridine → HCID 10056769, compound

https://huagongshe.com/reaction/233060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 10033903HCID 10033903—
SolventEthyl AcetateHCID 8857—
ProductHCID 10056769HCID 1005676976.2%

Reaction Steps

A solution of oxiranylmethyl [3,5-bis [[[2-(acetyloxy)-1-[(acetyloxy)methyl]ethyl]amino]carbonyl]-2,4,6-triiodophenyl]carbamate of Example 3a (12.1 g, 12.4 mmol) in freshly distilled anhydrous pyridine (120 ml) was heated at 75° C. for 45 minutes. Pyridine was removed under diminished pressure at 45° C. and the residue was co-evaporated twice with toluene (75 ml). The solid thus obtained was dissolved in ethyl acetate (250 ml) and the solution was washed with H2O (1×100 ml). The organic layer was dried (MgSO4). It was then filtered and the solvent removed to obtain the title compound as a yellow solid (9.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591846
Source datasetuspto-grants-1997_01
ORD IDord-9758480cdbce4fab839ab102470c48e2
Source noteuspto-grants-1997_01