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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565200Generated: October 29, 2026

Sodium Iodide → tert-Butyl piperazine-1-carboxylate

https://huagongshe.com/reaction/565200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant2,3-Dihydrobenzo[1,4]dioxine-5-carboxylic acid(piperidin-4-ylmethyl)amideHCID 15485934—
Reactant4-tert-Butoxycarbonyl-1-[(3-chloro-1-propyl)sulfonyl]piperazineHCID 22709890—
SolventDimethylformamideHCID 6228—
Producttert-Butyl piperazine-1-carboxylateHCID 143452193.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2,3-dihydrobenzo[1,4]dioxine-5-carboxylic acid(piperidin-4-ylmethyl)amide (28.6 g, 104 mmol), 4-(3-chloropropane-1-sulfonyl)piperazine-1-carboxylic acid tert-butyl ester (33.9 g, 104 mmol), sodium iodide (7.8 g, 52 mmol), and triethylamine (29 mL, 209 mmol) in N,N-dimethylformamide (70 mL) was stirred at 90° C. for 4 hours. The cooled reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with water (three times) and brine, dried (Na2SO4) and the solvents evaporated in vacuo. The crude product was purified by silica gel chromatography (5% methanol-dichloromethane) and crystallization from ethyl acetate-hexane to give 4-[3-(4-{[2,3-dihydrobenzo[1,4]dioxin-5-carbonyl)amino]-methyl}piperidin-1-yl)propane-1-sulfonyl]piperazine-1-carboxylic acid tert-butyl ester (37.5 g, 64%); m.p. 130-132° C. Analysis for C27H43N4O7 S: Calcd.: C, 57.12; H, 7.63; N, 9.87. Found: C, 57.01; H, 7.40; N, 9.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172062B2
Source datasetuspto-grants-2001_01
ORD IDord-022893ad69904bbaa3719462a07a4ca1
Source noteuspto-grants-2001_01