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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323650Generated: October 29, 2026

Acetyl chloride → HCID 22006271, compound

https://huagongshe.com/reaction/323650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2,6-LutidineHCID 7937—
ReactantHCID 178426276HCID 178426276—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 22006271HCID 2200627162%

Reaction Steps

A suspension of the 7-chloro-4-hydroxy-2-(4′-methylphenyl)-5,10-dihydro-2H-pyridazino[4,5-b]quinoline-1-one (755 mg), acetyl chloride (0.205 mL) and 2,6-lutidine (0.337 mL) was refluxed in toluene (6 mL) for 2 hours. The resulting mixture was cooled to room temperature. The resulting paste was diluted with ether (15 mL) and filtered in vacuo. The solids were washed with ether and ethyl acetate. The crude solids were triturated in warm ethyl acetate, then cooled to room temperature and filtered in vacuo. After drying this afforded the title compound as a light yellow solid (528 mg, 62%). mp 238-240° C.; MS 382 (m+H); NMR 2.34(s,3H), 2.41(s,3H), 3.85(s, 2H), 6.98(dd,1H,J1=8.1,J2=1.9), 7.09(d,1H,J=1.9), 7.18(d,1H,J=8.1), 7.28(d,2H,J=8.3), 7.39(d,2H,J=8.3), 9.06(s,1H); Analysis C20H16ClN3O3. 0.03M H2O expected/theoretical C 62.09/62.04H 4.24/2.27 N 10.62/10.85.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214826B1
Source datasetuspto-grants-2001_04
ORD IDord-93e156d51cc24d58afe5e7eaa4073c99
Source noteuspto-grants-2001_04