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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870748Generated: October 30, 2026

(5S)-5-(Aminomethyl)pyrrolidin-2-one → HCID 86696454, compound

https://huagongshe.com/reaction/870748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5S)-5-(Aminomethyl)pyrrolidin-2-oneHCID 14143191—
Reactant3-Bromo-6-fluoroimidazo[1,2-b]pyridazineHCID 86696318—
ProductHCID 86696454HCID 8669645462%

Reaction Steps

The (S)-5-(aminomethyl)pyrrolidin-2-one was reacted with 3-bromo-6-fluoroimidazo[1,2-b]pyridazine under the amine displacement conditions described in example 5.6.42, Part A, to obtain the titled in 62% yield. 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.90-2.04 (m, 1H) 2.24-2.50 (m, 3H) 3.46-3.56 (m, 2H) 4.09 (quin, J=5.84 Hz, 1H) 6.74 (d, J=9.70 Hz, 1H) 7.43 (s, 1H) 7.60 (d, J=9.70 Hz, 1H); LRMS (ESI) m/310.0 doublet [(M+H)+, calcd for C11H12BrN5O 309.0].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-5fc4842091f74440a0af22c838b11a72
Source noteuspto-grants-2015_03