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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133524Generated: October 25, 2026

1-(2-Methyl-4-phenyl-5,6,7,8-tetrahydro-9-thia-1,7-diaza-fluoren-3-yl)-ethanone → 1-(2-Methyl-4-phenyl-9-thia-1,7-diaza-fluoren-3-yl)-ethanone

https://huagongshe.com/reaction/133524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methyl-4-phenyl-5,6,7,8-tetrahydro-9-thia-1,7-diaza-fluoren-3-yl)-ethanoneHCID 68896554—
CatalystPalladiumHCID 23938—
SolventStilbeneHCID 11502—
Product1-(2-Methyl-4-phenyl-9-thia-1,7-diaza-fluoren-3-yl)-ethanoneHCID 1155146811%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a stirred solution of 0.70 g (2.17 mmol) 1-(2-methyl-4-phenyl-5,6,7,8-tetrahydro-9-thia-1,7-diaza-fluoren-3-yl)-ethanone in 10 ml diphenylethylene was added 325 mg palladium on charcoal 10%. The mixture was stirred over night at 150° C., and then poured onto ethyl acetate (about 150 ml), and extracted three times aqueous HCl (1M). The combined aqueous phases were basified with K2CO3 until ph=8, and then the product was extracted with ethyl acetate. The combined organic phase were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 1:1) afforded 75 mg (11%) 1-(2-methyl-4-phenyl-9-thia-1,7-diaza-fluoren-3-yl)-ethanone as a light yellow solid. ES-MS m/e (%): 319 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390903B2
Source datasetuspto-grants-2008_06
ORD IDord-14452336198b4e7584a35ac75d147b6a
Source noteuspto-grants-2008_06