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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408944Generated: November 1, 2026

6-Bromo-4-(3-hydroxy-2,2-dimethylcyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide → 6-Bromo-4-(2,2-dimethyl-3-oxocyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide

https://huagongshe.com/reaction/1408944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-(3-hydroxy-2,2-dimethylcyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamideHCID 68291072—
Reactant4-[(2,2-Dimethyl-3-oxocyclopentyl)amino]pyrrolo[1,2-b]pyridazine-3-carboxamideHCID 68358619—
Product6-Bromo-4-(2,2-dimethyl-3-oxocyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamideHCID 6829116781.4%

Reaction Steps

Following conditions described in Step 1 of Intermediate 22, 6-bromo-4-(3-hydroxy-2,2-dimethylcyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide (395 mg, 1.076 mmol, from Step 1) was converted to 6-bromo-4-(2,2-dimethyl-3-oxocyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide (320 mg, 80% yield). 1H NMR (400 MHz, methanol-d4) δ ppm 8.19 (1 H, s), 7.69 (1 H, d, J=1.76 Hz), 7.16 (1 H, d, J=1.76 Hz), 2.36-2.73 (3 H, m), 1.89-2.06 (1 H, m), 1.15 (6 H, s); MS (ES+) m/z: 365.2, 367.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921368B2
Source datasetuspto-grants-2014_12
ORD IDord-80e096c31a9844858895375f7159fdb4
Source noteuspto-grants-2014_12