Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903082Generated: November 1, 2026

Triethylamine → HCID 20437729, compound

https://huagongshe.com/reaction/1903082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Chloro-6-methoxypyridazineHCID 74403—
Reactant2-(1-Piperazinyl)-4-amino-6,7-dimethoxyquinazolineHCID 616267—
Solvent1-PentanolHCID 6276—
ProductHCID 20437729HCID 20437729—

Reaction Steps

4-Amino-6,7-dimethoxy-2-piperazinoquinazoline (3.0 g, 10.4 mmole), 3-chloro-6-methoxy-pyridazine (3.96 g, 27.4 mmole) and triethylamine (5.0 g, 49.5 mmole) in n-pentanol (210 ml) were heated under reflux for 25 hours. The solvent was evaporated in vacuo and the residue partitioned between chloroform and saturated aqueous sodium carbonate solution. The organic layer was separated, washed with water, dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica gel (200 g) eluting with chloroform followed by 5% methanol in chloroform. Further purification of the major product by HPLC using a Waters 500 Prep. LC/system, eluting with 6% by volume methanol in methylene chloride at a flow rate of 0.15 liters per minute gave the desired product which was recrystallized from methanol, m.p. 269°-270° C. (0.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435401
Source datasetuspto-grants-1984_03
ORD IDord-a1f811f12ebd440b8b8125204f836e4b
Source noteuspto-grants-1984_03