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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435593Generated: October 29, 2026

Methane → HCID 21455932, compound

https://huagongshe.com/reaction/435593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantHCID 21455926HCID 21455926—
ProductHCID 21455932HCID 21455932—

Reaction Steps

1.8 g. 3-(5-nitro-1-β-acetoxyethyl-2-imidazolyl)-6-(4-methyl-1 -piperazinyl)-s-triazolo[4,3-b]pyridazine (obtained according to Example 23) was reacted for 1.5 hours at 50° C. with 36 ml. 2N hydrochloric acid. The solution was then treated with charcoal, evaporated in a vacuum and the residue dissolved in 10 ml. water, adjusted to about pH 9 with concentrated aqueous ammonia, left to stand for about 30 minutes and the precipitated crystals were filtered off with suction and washed with water and ether. There was thus obtained 1.1 g. of the desired 3-(5-nitro- 1-β-hydroxyethyl-2-imidazolyl)-6-(4-methyl-1-piperazinyl)-s-triazolo[ 4,3-b]pyridazine. After drying for 1.5 days in a vacuum at 70°C., the product has a melting point of 98° - 100° C. (foams up).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006141
Source datasetuspto-grants-1977_02
ORD IDord-28c40b17058f42e997a0e0cfbe7980b9
Source noteuspto-grants-1977_02