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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406134Generated: November 1, 2026

Hydrazine → HCID 12582745, compound

https://huagongshe.com/reaction/2406134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHCID 20441588HCID 20441588—
SolventPyridineHCID 1049—
ProductHCID 12582745HCID 12582745—

Reaction Steps

3-Chloro-5,6,7,8,9,10-hexahydrocycloocta[c]pyridazine (1.36 g) was treated with anhydrous pyridine (10 mL) and anhydrous hydrazine (3 mL) at 100° C. for 5.5 h. The solvent was removed under vacuum and the residue was partitioned between chloroform and saturated aqueous potassium carbonate solution. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum to provide 3-hydrazinyl-5,6,7,8,9,10-hexahydrocycloocta[c]pyridazine; 1H NMR (CDCl3, 300 MHz) 6.71 (s, 1H), 3.01 (m, 2H), 2.68 (m, 2H), 1.70-1.85 (m, 4H), 1.40 (m, 4H) ppm; MS (ES) 193 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809347B2
Source datasetuspto-grants-2014_08
ORD IDord-e924e28c20fb4709a2158b463ee7022f
Source noteuspto-grants-2014_08