HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760044Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 69745485, compound
https://huagongshe.com/reaction/1760044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | HCID 22599906 | HCID 22599906 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 69745485 | HCID 69745485 | 27% |
Reaction Steps
Anhydrous potassium carbonate (640 mg, 4.63 mmol) and 2-fluoronitrobenzene (820 mg, 5.81 mmol) were added to a dimethyl sulfoxide (100 ml) solution of N-(2-amino-3,3-dimethylbutyryl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (1.05 g, 3.42 mmol) obtained in Reference example 7, and the mixture was heated at 80° C. for 90 minutes. The reaction mixture was cooled to room temperature, diluted with a diethyl ether solution (200 ml), washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography using ethyl acetate and hexane (1:4 to 2:1) as an eluent to obtain the captioned compound (395 mg, 27%) as an orange foamy substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838465B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-40ed47afac5b49fdaf959051f95f3ee6 |
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| Source note | uspto-grants-2005_01 |
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