HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222059Generated: October 30, 2026
Potassium tert-butoxide → HCID 178480890, compound
https://huagongshe.com/reaction/222059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 67311978 | HCID 67311978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178480890 | HCID 178480890 | 114.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207172B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-7601d154690c4118a50c16fe91f13e33 |
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| Source note | uspto-grants-2012_06 |
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