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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890194Generated: October 30, 2026

Iodine → (4-Iodo-pyridin-3-YL)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/890194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactantn-Butyl lithiumHCID 61028—
Reactant3-(Boc-amino)pyridineHCID 10932321—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product(4-Iodo-pyridin-3-YL)-carbamic acid tert-butyl esterHCID 1536641361.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

N-Butyllithium (1.6M hexane solution 400 mL, 0.64 mol) was added to a solution of tert-butyl N-(3-pyridyl)carbamate (51.8 g, 0.27 mol) and tetramethylethylenediamine (96.6 mL, 0.64 ml) in diethyl ether (1.5 L) at −78° C., followed by stirring at −20° C. for 2.5 hr. After cooling to −78° C. again, a solution of iodine (94.8 g, 0.37 mol) in diethyl ether (200 mL) was added and stirred for one day while raising a temperature to room temperature. Water was added, extracted with diethyl ether, and the organic layer was washed with hypo-water and brine, dried over anhydrous magnesium sulfate and evaporated. The resulting crystals were washed with hexane, to give the title compound (53.0 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995163B2
Source datasetuspto-grants-2006_02
ORD IDord-6f676df94e5946cf89a8b5a5e16dccd7
Source noteuspto-grants-2006_02