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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654101Generated: October 29, 2026

Sodium Bicarbonate → 1-[3-(4-(5-fluoro-3-indolyl)-1,2,3,6-tetrahydro-1-pyridyl)propyl]-5,6-dihydro(1H,4H)-1,2,5-thiadiazolo[4,3,2-ij]quinoline 2,2-dioxide

https://huagongshe.com/reaction/654101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 11344959—
Reactant1-(3-chloropropyl)-5,6-dihydro(1H,4H)-1,2,5-thiadiazolo[4,3,2-ij]quinoline 2,2-dioxideHCID 19888450—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-[3-(4-(5-fluoro-3-indolyl)-1,2,3,6-tetrahydro-1-pyridyl)propyl]-5,6-dihydro(1H,4H)-1,2,5-thiadiazolo[4,3,2-ij]quinoline 2,2-dioxideHCID 1988846440.4%

Reaction Steps

The operation is as in Example 3, starting with 1-(3-chloropropyl)-5,6-dihydro(1H,4H)-1,2,5-thiadiazolo[4,3,2-ij]quinoline 2,2-dioxide (3.8 g), 4-(5-fluoro-3-indolyl)-1,2,3,6-tetrahydropyridine (2.9 g) and sodium bicarbonate (3.3 g) in a mixture of dimethylformamide (40 cc) and tetrahydrofuran (25 cc). The mixture is heated to boiling for 48 hours and is then cooled to a temperature close to 20° C. After purification by flash chromatography on a silica column, under a stream of argon at moderate pressure (0.5-1.5 bars) with ethyl acetate as eluent and recrystallization from boiling acetonitrile (200 cc), 1-[3-(4-(5-fluoro-3-indolyl)-1,2,3,6-tetrahydro-1-pyridyl)propyl]-5,6-dihydro(1H,4H)-1,2,5-thiadiazolo[4,3,2-ij]quinoline 2,2-dioxide (2.5 g) is obtained, melting at 178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130313
Source datasetuspto-grants-1992_07
ORD IDord-567a51a500d9415c8faa4d4cb24e9a59
Source noteuspto-grants-1992_07