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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076665Generated: November 2, 2026

Dimethylformamide → HCID 68138851, compound

https://huagongshe.com/reaction/1076665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDimethylformamide diethylacetalHCID 70913—
ReactantHCID 21537442HCID 21537442—
ProductHCID 68138851HCID 68138851—

Reaction Steps

0.8 g. 3-(5-nitro-2-thienyl)-6-amino-s-triazolo[4,3-b]pyridazine was suspended in a mixture of 3 ml. N,N-dimethylformamide and 1. ml. N,N-dimethyl formamide-diethyl acetal and heated, while stirring, on a waterbath for two hours. Thereafter, the reaction mixture was cooled, solid material was filtered off with suction and the residue is washed with N,N-dimethyl formamide. There was thus obtained 0.4 g. (41% of theory) 3-(5-nitro-2-thienyl)-6-(diethylaminomethylene)-amino-s-triazolo[4,3-b]pyridazine (m.p. 247°-249°C). After recrystallization from N,N-dimethyl-formamide, with the addition of charcoal the product was obtained in the form of yellow crystals which melt at 249°-252°C. The elementary analyses and spectra confirm the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957766
Source datasetuspto-grants-1976_05
ORD IDord-990c6c3873d448a9bc6d149f641007d7
Source noteuspto-grants-1976_05