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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408920Generated: November 1, 2026

(1R)-2,2-dimethylcyclopentan-1-amine → (R)-Ethyl 3-carbamoyl-4-((2,2-dimethylcyclopentyl)amino)pyrrolo[1,2-b]pyridazine-6-carboxylate

https://huagongshe.com/reaction/1408920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R)-2,2-dimethylcyclopentan-1-amineHCID 15196533—
ReactantEthyl 3-carbamoyl-4-chloropyrrolo[1,2-b]pyridazine-6-carboxylateHCID 68290691—
Reactant4, 6-Dichloropyrrolo[1,2-b]pyridazine-3-carboxamideHCID 68291540—
Product(R)-Ethyl 3-carbamoyl-4-((2,2-dimethylcyclopentyl)amino)pyrrolo[1,2-b]pyridazine-6-carboxylateHCID 68358891—

Reaction Steps

Prepared by reacting (R)-2,2-dimethylcyclopentylamine with ethyl 3-carbamoyl-4-chloropyrrolo[1,2-b]pyridazine-6-carboxylate (Preparation 4) according to the procedure described in Step 5 of Intermediate 4. HPLC (condition B): retention time=3.67 min. LCMS (condition E): m/z 345+ve. 1H NMR (400 MHz, MeOD) δ ppm 10.86 (1 H, br. s.), 8.20 (1 H, s), 8.01 (1 H, d, J=1.76 Hz), 7.38 (1 H, d, J=1.54 Hz), 4.27-4.43 (2 H, m), 4.13-4.29 (1 H, m), 2.29-2.46 (1 H, m), 1.58-1.92 (5 H, m), 1.38 (3 H, t, J=7.15 Hz), 1.13 (3 H, s), 1.10 (3 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921368B2
Source datasetuspto-grants-2014_12
ORD IDord-e84a504955824ac4b3d93caacde6fc97
Source noteuspto-grants-2014_12