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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661828Generated: October 28, 2026

3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine → HCID 57654475, compound

https://huagongshe.com/reaction/1661828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazineHCID 54595607—
ReactantHCID 57654572HCID 57654572—
Solvent1-ButanolHCID 263—
ProductHCID 57654475HCID 576544757%

Reaction Steps

Quinazolin-6-yl-acetic acid hydrazide (0.032 g, 0.158 mmol) and 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-pyridazine (0.031 g, 0.158 mmol) were heated to 165° C. in butanol (2 mL) for five hours. The reaction was cooled to room temperature, evaporated in vacuo and purified via silica gel column chromatography eluting with 5% methanol in dichloromethane to give 0.0031 g (7%) of 6-[6-(1-methyl-1H -pyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl]-quinazoline. 1H NMR (400 MHz, CD3OD) δ 8.45 (s, 1H), 8.29 (s, 1H), 8.06 (d, 2H, J=9.6 Hz), 7.60 (d, 2H, J=9.6 Hz), 7.55 (m, 1H), 7.17 (d, 1H, J=8.0 Hz), 6.08 (s, 1H), 4.58 (m, 2H), 3.89 (s, 3H). Mass spectrum (LCMS, ESI pos.): Calcd for C18H14N8; found: 343.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030305B2
Source datasetuspto-grants-2011_10
ORD IDord-dda9b6f596ac44fb8c42e081ca6c5fd1
Source noteuspto-grants-2011_10