HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604277Generated: October 29, 2026
Potassium Carbonate → 4-[1-(2-Methyl-8-nitro-1-oxo-1,2,3,4-tetrahydro-isoquinolin-5-yl)-piperidin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/604277
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 4-(piperidin-4-yl)piperazine-1-carboxylate | HCID 17750356 | — |
| Reactant | 5-fluoro-2-methyl-8-nitro-3,4-dihydro-2H-isoquinolin-1-one | HCID 59849176 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[1-(2-Methyl-8-nitro-1-oxo-1,2,3,4-tetrahydro-isoquinolin-5-yl)-piperidin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester | HCID 59849170 | 41% |
Reaction Steps
A mixture of 5-fluoro-2-methyl-8-nitro-3,4-dihydro-2H-isoquinolin-1-one (11.65 g, 0.052 mol), 4-piperidin-4-yl-piperazine-1-carboxylic acid tert-butyl ester (28.0 g, 0.1039 mol), K2CO3 (8.98 g, 0.065 mol) in DMSO (350 mL) was stirred at 85° C. for 12 hours. After cooling to room temperature, ice-water (500 mL) was added. The mixture was extracted with AcOEt. The organic layer was washed with water followed by brine, dried over Na2SO4 and evaporated. The residue was purified by silica gel column chromatography (AcOEt; then AcOEt/MeOH=6/1) to give 10.09 g of the desired product 4-[1-(2-methyl-8-nitro-1-oxo-1,2,3,4-tetrahydro-isoquinolin-5-yl)-piperidin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester as pale yellow solid in 41% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910585B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-ebeaa36887304526a75545382def6811 |
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| Source note | uspto-grants-2011_03 |
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