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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865362Generated: November 1, 2026

Iodine → HCID 10476981, compound

https://huagongshe.com/reaction/865362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPyridineHCID 1049—
ReactantHCID 9977053HCID 9977053—
SolventChloroformHCID 6212—
ProductHCID 10476981HCID 10476981—

Reaction Steps

N-Allyl-N-carbobenzyloxy-4-(3-pyridyl)-3,5-difluoroaniline (PREPARATION 4, 496 mg 1.31 mmol) in chloroform (25 ml), pyridine (1.58 ml, 19.6 mmol, 15 eq) and iodine (4.97 g, 19.6 mmol, 15 eq) are combined. The resulting mixture is placed under an atmosphere of nitrogen and heated to 50° with stirring. After 1.5 hr, the reaction is decanted into chloroform (70 ml). The remaining sludge is rinsed with chloroform (3×15 ml). The combined organics are washed with sodium thiosulfate (20%), then brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to give a solid. This material is purified by silica gel chromatography (100 g) eluting with methanol/chloroform (0.5/99.5 - 11, 1/99, 11). The appropriate fractions are pooled and concentrated to give the title compound, mp 133°-134°; FTIR (mull) cm-1 3130, 1758, 1650, 1414, 1241, 1017 and 846; NMR (CDCl3) 8.72, 8.62, 7.79, 7.43-7.38, 7.32, 4.84-4.72, 4.19, 3.80, 3.51 and 3.39 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565571
Source datasetuspto-grants-1996_10
ORD IDord-8b825c4570084cebb5de7a39bb81d5a1
Source noteuspto-grants-1996_10