HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595116Generated: October 29, 2026
2-Bromo-4-fluorobenzene-1-sulfonyl chloride → Methyl 8-(2-bromo-4-fluorobenzenesulfonylamino)-5,6-dihydropyrazolo[5,1-a]isoquinoline-7-carboxylate
https://huagongshe.com/reaction/595116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-4-fluorobenzene-1-sulfonyl chloride | HCID 2778216 | — |
| Reactant | Methyl 8-amino-5,6-dihydropyrazolo[5,1-a]isoquinoline-7-carboxylate | HCID 86712823 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 8-(2-bromo-4-fluorobenzenesulfonylamino)-5,6-dihydropyrazolo[5,1-a]isoquinoline-7-carboxylate | HCID 70984117 | 74.3% |
Reaction Steps
A mixture of methyl 8-amino-5,6-dihydropyrazolo[5,1-a]isoquinoline-7-carboxylate (Intermediate 22, 0.060 g) and 2-bromo-4-fluorobenzenesulfonyl chloride (0.081 g) in pyridine (2 mL) and DCM (4 mL) was stirred at room temperature overnight. A further amount of 2-bromo-4-fluoro-benzenesulfonyl chloride (0.010 g) was added and the reaction mixture was stirred at room temperature for 2 hours. The resultant mixture was concentrated in vacuo and the residue was dissolved in DCM and washed with 1M hydrochloric acid, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-100% to give methyl 8-(2-bromo-4-fluorobenzenesulfonylamino)-5,6-dihydropyrazolo[5,1-a]isoquinoline-7-carboxylate (0.088 g) as a glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09242997B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-28c7ebc6296d4abaa731905a3c65db85 |
|---|
| Source note | uspto-grants-2016_01 |
|---|