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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222059Generated: October 30, 2026

Potassium tert-butoxide → HCID 178480890, compound

https://huagongshe.com/reaction/222059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67311978HCID 67311978—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178480890HCID 178480890114.2%

Reaction Steps

To a yellow suspension of 3-[2-(4-methyl-piperazin-1-yl)-ethyl]-6-[2-(4-nitro-phenyl)-ethoxy]-4,5-dihydro-3H-10-thia-2,3,7,9-tetraaza-cyclopenta[a]fluorene (2.7 g, 5.2 mmol) in THF (125 ml) was added potassium tert-butoxide (0.92 g, 7.79 mmol) in one portion. The reaction mixture became a solution and then turned into a dark black solution. After stirring for 30 min, analytical HPLC showed no more starting material and two new major peaks. Solvents were evaporated and the dark residue was suspended in EtOAc. To above suspension was added 5 ml of 4M HCl and it turned into a light yellow suspension. The crude HCl salt of the desired product was collected by filtration, washed with EtOAc, and air-dried to afford the crude product (2.2 g, 104%). RT=0.41 min; [M+H]+=371.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207172B2
Source datasetuspto-grants-2012_06
ORD IDord-7601d154690c4118a50c16fe91f13e33
Source noteuspto-grants-2012_06