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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224284Generated: November 1, 2026

Triphosgene → HCID 59716808, compound

https://huagongshe.com/reaction/2224284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantHCID 59716608HCID 59716608—
ReactantHCID 86599008HCID 86599008—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59716808HCID 59716808—

Reaction Steps

A stirring solution of triphosgene (19.0 g, 64.0 mmol) in THF (200 mL) was cooled to 0° C. under argon and the mixture of 1-(4-chloro-5-p-tolylpyridazin-3-yl)hydrazine and 1-(3-chloro-5-p-tolylpyridazin-4-yl)hydrazine (3.0 g gross), prepared as described in Example 362C, was added over 3 min. The reaction mixture was allowed to warm to RT gradually and then stirred for 16 h. Solvent was removed under vacuum to reduce the reaction mixture to half its original volume, and the resulting suspension was cooled to an ice bath. Ice water (300 mL) was added, followed by stirring for 1 h. The product was collected by filtration and washed with 0.1 M aqueous HCl (50 mL×2), then H2O (50 mL×2). After drying under vacuum at 50° C. for 2 d, the title compound, 8-chloro-7-p-tolyl-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one, (2.2 g) was obtained as a yellow solid. MS [M+H]+ 261; HPLC retention time=2.75 min; 1HNMR (400 MHz, THF-d8) δ 11.69 (s, 1H), 8.10 (s, 1H), 7.49-7.51 (m, 2H), 7.34-7.35 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-5543b71ab48e46f3a195219e8437d393
Source noteuspto-grants-2008_05