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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | n-Butyl lithium | HCID 61028 | — |
| Reactant | 3-(Boc-amino)pyridine | HCID 10932321 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-Iodo-pyridin-3-YL)-carbamic acid tert-butyl ester | HCID 15366413 | 61.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06995163B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-6f676df94e5946cf89a8b5a5e16dccd7 |
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| Source note | uspto-grants-2006_02 |
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