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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637639Generated: October 29, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → [2-(1H-Benzimidazol-2-ylsulfanylmethyl)-3-chloro-pyridin-4-yl]methyl-[2-(3-nitroimidazo[1,2-b]pyridazin-6-ylsulfanyl)ethyl]amine

https://huagongshe.com/reaction/1637639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-chloropyridin-4-yl]-(2-chloroethyl)methyl-amineHCID 53762852—
ReactantHCID 178526776HCID 178526776—
SolventDimethylformamideHCID 6228—
Product[2-(1H-Benzimidazol-2-ylsulfanylmethyl)-3-chloro-pyridin-4-yl]methyl-[2-(3-nitroimidazo[1,2-b]pyridazin-6-ylsulfanyl)ethyl]amineHCID 7027295966.4%

Reaction Steps

0.44 g (1.0 mmol) of [2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-chloropyridin-4-yl]-(2-chloroethyl)methyl-amine, 0.24 g (1.2 mmol) of 3-nitroimidazo[1,2-b]pyridazine-6-thiol and 0.52 ml (3.5 mmol) of DBU are reacted in 10 ml of dimethylformamide by the procedure described in Example 16. After crystallization from diisopropyl ether, 0.35 g (66%) of the title compound is obtained as a pale beige solid. M.p. 184-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043242
Source datasetuspto-grants-2000_03
ORD IDord-f94b071998c5424a8558987538b87889
Source noteuspto-grants-2000_03