Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870720Generated: November 2, 2026

N,N'-Dimethylethylenediamine → HCID 86696424, compound

https://huagongshe.com/reaction/870720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantSodium CyanideHCID 8929—
ReactantHCID 86696425HCID 86696425—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 86696424HCID 8669642425%

Reaction Steps

A solution of (S)-iso-propyl 2-(((3-bromoimidazo[1,2-b]pyridazin-6-yl)amino)methyl)pyrrolidine-1-carboxylate (300 mg, 0.79 mmol), NaCN (46 mg, 0.94 mmol), CuI (15 mg, 0.08 mmol), KI (27 mg, 0.16 mmol) and N1,N2-dimethylethane-1,2-diamine (0.085 mL, 0.79 mmol) in toluene (0.8 mL) was stirred at 110° C. for 12 h. The reaction was cooled, concentrated, taken up with EtOAc and water, extracted and dried organic layer with MgSO4. The organic layer was concentrated and purified by ISCO (0-5% MeOH/DCM), then following PREP HPLC (neutral) to give (S)-isopropyl 2-(((3-cyanoimidazo[1,2-b]pyridazin-6-yl)amino)methyl)pyrrolidine-1-carboxylate (63 mg, 25% yield). 1H NMR (400 MHz, METHANOL-d4) δ ppm 8.00 (s, 1H), 7.72 (d, J=9.85 Hz, 1H), 6.91 (d, J=9.85 Hz, 1H), 4.20 (m, 1H), 3.38-3.61 (m, 4H), 1.97-2.05 (m, 4H), 1.16-1.25 (m, 6H); LRMS (ESI) m/e 329.2 [(M+H)+, calcd for C16H21N6O2 329.4].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-90684c4ce0a94042a87ba2e358b23aa0
Source noteuspto-grants-2015_03