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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097301Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 59708795, compound

https://huagongshe.com/reaction/1097301

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 59708794HCID 59708794—
SolventDichloromethaneHCID 6344—
ProductHCID 59708795HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143256B2
Source datasetuspto-grants-2012_03
ORD IDord-b3237dafee7c450e969b43f7562c7c55
Source noteuspto-grants-2012_03