Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597921Generated: October 29, 2026

Pyridine → HCID 9798097, compound

https://huagongshe.com/reaction/1597921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
Reactant6-Chloro-2,3-dihydro-1H-indole--hydrogen chloride (1/1)HCID 18932875—
SolventIsopropanolHCID 3776—
ProductHCID 9798097HCID 9798097—

Reaction Steps

To 6-chloroindoline hydrochloride (1 00 mg, 0.526 mmol) and pyridine (0.957 mmol, 77 μL) in dry i-PrOH (8 mL) was added 4-chloro-6,7-dimethoxyquinazoline (107 mg, 0.478 mmol). The mixture was refluxed for 2 hours under an atmosphere of dry N2(g) and then the solvent was removed in vacuo. The residue was partitioned between CHCl3 and 1M NaOH, and the organic phase was washed with brine, dried over Na2SO4(g) and concentrated in vacuo. The residue (171 mg) was purified by flash chromatography on silica using 80%EtOAc/CH2 Cl2 to yield 4-(6-chloro-2,3-dihydro-indol-1-yl)-6,7-dimethoxy-quinazoline as its free base (148 mg) (M.P. 229°-230° C.; LC-MS: 342 (MH+); anal. RP18-HPLC RT: 4.38 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736534
Source datasetuspto-grants-1998_04
ORD IDord-f3ebcff4d1714bed8453c727bcd8bc72
Source noteuspto-grants-1998_04