HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097301Generated: October 30, 2026
1,1'-Carbonyldiimidazole → HCID 59708795, compound
https://huagongshe.com/reaction/1097301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | HCID 59708794 | HCID 59708794 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59708795 | HCID 59708795 | — |
Reaction Steps
1,1′-Carbonyldiimidazole (129 mg, 0.796 mmol) was added to a solution of 5-[4-(4-tert-butoxycarbonylaminobutyl)piperazin-1-yl]pentanoic acid (111) (219 mg, 0.613 mmol) in anhydrous dichloromethane (8 mL) and the mixture was stirred at room temperature for 2 hours. N-Boc piperazine (148 mg, 0.796 mmol) was then added in one portion and the reaction mixture was stirred at room temperature for an additional 16 hours. The mixture was then concentrated under reduced pressure, and the resulting residue was purified by Biotage silica gel column chromatography using methanol/dichloromethane (gradient 0% to 2%) to give 4-{5-[4-(4-tert-butoxycarbonylaminobutyl)piperazin-1-yl]pentanoyl}piperazine-1-carboxylic acid tert-butyl ester 112 as a viscous, yellow oil (309 mg, 96%): 1H NMR (500 MHz, CDCl3) δ 1.44 (s, 9H), 1.48 (s, 9H), 1.55 (m, 6H), 1.66 (m, 2H), 2.35 (m, 8H), 2.48 (m, 6H), 3.11 (m, 2H), 3.40 (m, 2H), 3.44 (m, 4H), 3.58 (m, 2H), 5.30 (br, 1H). m/z (ESI) 526 [C27H51N5O5+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143256B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-b3237dafee7c450e969b43f7562c7c55 |
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| Source note | uspto-grants-2012_03 |
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