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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597919Generated: October 31, 2026

Pyridine → HCID 53754941, compound

https://huagongshe.com/reaction/1597919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant6-Chloro-2,3-dihydro-1h-indoleHCID 258567—
Reactant4-Chloro-7,8-dihydro[1,4]dioxino[2,3-g]quinazolineHCID 18932867—
SolventIsopropanolHCID 3776—
ProductHCID 53754941HCID 5375494187%

Reaction Steps

To 6-chloroindoline (52 mg, 0.339 mmol) and pyridine (23.3 mg, 0.294 mmol) in i-PrOH (3 mL) was added 4-chloro-6,7-(ethylenedioxy)quinazoline (65 mg, 0.284 mmol). The mixture was heated to reflux under dry N2(g) for 16 hours and then concentrated in vacuo. The residue was partitioned between CHCl3 and saturated aqueous NaHCO3, and the organic phase was washed with brine, dried over Na2SO4(s), and concentrated in vacuo. The residue was flash chromatographed on silica using 30% acetone/hexanes to afford 84 mg of 4-(6-chloro-2,3-dihydro-indol-1-yl)-7,8-dihydro-[1,4]dioxino [2,3-g]quinazoline as its free-base (M.P. 209°-211° C.; GC/MS: 339 (M+); anal. RP18-HPLC RT: 5.02 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736534
Source datasetuspto-grants-1998_04
ORD IDord-c77206b4a7914c38b338918d8d8cc20c
Source noteuspto-grants-1998_04