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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890951Generated: November 1, 2026

Carbon Disulfide → HCID 178504226, compound

https://huagongshe.com/reaction/1890951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium CarbonateHCID 11430—
Reactant{6-[1-(2-Trimethylsilanyl-ethoxymethyl)-1H-pyrazol-4-yl]-pyridazin-3-yl}-hydrazineHCID 68975416—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178504226HCID 178504226—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of {6-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-4-yl]-pyridazin-3-yl}-hydrazine (490 mg, 1.6 mmol) in ethanol (6.5 mL) and water (1.8 mL) was added K2CO3 (359 mg, 2.6 mmol), followed by CS2 (0.212 mL, 3.5 mmol). The mixture was stirred and heated at 80° C. for 3 h under nitrogen atmosphere. The mixture was cooled to room temperature and concentrated to 50% volume in vacuo and acidified to pH 1 with 1 N aqueous HCl. The resulting precipitate was collected, washed with water, and dried in vacuo to provide title compound as a dark red solid (quantitative yield): 1H NMR (DMSO-d6) δ 0.01 (9H, s), 0.90 (2H, t), 3.63 (2H, t), 5.56 (2H, s), 7.82 (1H, d), 8.24 (1H, d), 8.27 (1H, s), 8.80 (1H, s), 15.23 (1H, bs); MS (m/z) 349 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507489B2
Source datasetuspto-grants-2013_08
ORD IDord-1bef38ff57354014950cc9e49ea2df5f
Source noteuspto-grants-2013_08