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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097299Generated: October 30, 2026

Sodium Iodide → HCID 59708792, compound

https://huagongshe.com/reaction/1097299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 5-bromovalerateHCID 84580—
Reactant1-(4-Boc-aminobutyl)piperazineHCID 4134691—
SolventAcetoneHCID 180—
ProductHCID 59708792HCID 5970879256%

Reaction Steps

A mixture of (4-piperazin-1-yl-butyl)carbamic acid tert-butyl ester (17) (1.94 g, 7.54 mmol), sodium iodide (1.13 g, 7.54 mmol), potassium carbonate (3.13 g, 22.61 mmol), and 5-bromopentanoic acid ethyl ester (1.55 mL, 9.80 mmol) in acetone (60 mL) was stirred at reflux for 24 h. After removal of solvent by rotary evaporation, the resulting residue was diluted with dichloromethane and insoluble inorganics were filtered off. The liquid filtrate was concentrated in vacuo and the resulting residue was purified by Biotage silica gel column chromatography using methanol/dichloromethane (gradient 0% to 5%) to give a yellow oil, which was further purified by Biotage chromatography using ethyl acetate/dichloromethane (gradient 30% to 99%) to afford 18 as a yellow oil (1.62 g, 56%): 1H NMR (500 MHz, CDCl3) δ 1.27 (t, 3H), 1.43 (s, 9H), 1.52 (m, 6H), 1.65 (m, 2H), 2.34 (m, 6H), 2.48 (m, 6H), 3.11 (m, 2H), 4.12 (q, 2H), 5.21 (br, 1H); ESI MS m/z 386 [C20H39N3O4+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143256B2
Source datasetuspto-grants-2012_03
ORD IDord-f132e485dd4f4bdb8c4ad3331068733c
Source noteuspto-grants-2012_03