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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416894Generated: October 30, 2026

Diisopropylethylamine → HCID 46743364, compound

https://huagongshe.com/reaction/416894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(Bromomethyl)cyclobutaneHCID 2734658—
SolventDichloromethaneHCID 6344—
ProductHCID 46743364HCID 467433648.8%

Reaction Conditions

Temperature35 °C

Reaction Steps

Bromomethylcyclobutane (0.200 g, 1.34 mmol, 1 eq) was suspended in DCM (2 mL). DIPEA (0.59 mL, 3.35 mmol, 2.5 eq) was added dropwise, followed by N-Boc-piperazine (0.550 g, 2.95 mmol, 2.2. eq), and the reaction mixture was stirred at 35° C. for 2 h. The crude product was purified by column chromatography on a Biotage SP1 system (DCM/EtOAc; v/v 1:1) to give the title compound (0.030 g, 8.8%); 1H-NMR (500 MHz, CDCl3): δ 1.46 (s, 9H, C(CH3)3), 1.64-1.74 (m, 2H), 1.76-1.96 (m, 2H), 2.02-2.12 (m, 2H), 2.37 (t, J=5.0 Hz, 4H, piperazine N(CH2)2), 2.43 (d, J=7.0 Hz, 2H, NCH2), 2.55 (m, 1H, cyclobutyl CH), 3.43 (t, J=5.0 Hz, 4H, piperazine N(CH2)2); GC-MS (Cl, m/z): Rt=3.77 min—255 [(M+H)+, 100%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088761B2
Source datasetuspto-grants-2012_01
ORD IDord-ee0f291475c24be69fa2320b81cf5603
Source noteuspto-grants-2012_01