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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3-Dihydrobenzo[1,4]dioxine-5-carboxylic acid(piperidin-4-ylmethyl)amide | HCID 15485934 | — |
| Reactant | 4-tert-Butoxycarbonyl-1-[(3-chloro-1-propyl)sulfonyl]piperazine | HCID 22709890 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl piperazine-1-carboxylate | HCID 143452 | 193.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172062B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-022893ad69904bbaa3719462a07a4ca1 |
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| Source note | uspto-grants-2001_01 |
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