HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014372Generated: October 30, 2026
HCID 59441905, compound → HCID 59442020, compound
https://huagongshe.com/reaction/1014372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59441905 | HCID 59441905 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59442020 | HCID 59442020 | 96.1% |
Reaction Steps
6-(methyloxy)-2-(1-methylpropyl)-7-nitro-1,2,3,4-tetrahydroisoquinoline (0.23 g, 0.87 mmol) was dissolved in ethyl acetate (5 mL), treated with 10% palladium on carbon (50 mg, Aldrich), and then diluted with methanol (10 mL). The mixture was stirred under 60 psi of hydrogen pressure for 16 h in a Fischer-Porter apparatus. The pressure was released, the reaction vessel evacuated, and back-filled with nitrogen twice. The mixture was filtered through celite and the filtrate was concentrated to provide 6-(methyloxy)-2-(1-methylpropyl)-1,2,3,4-tetrahydro-7-isoquinolinamine (196 mg, 96%). 1H NMR (400 MHz, CDCl3) δ ppm 0.90 (t, J=7.4 Hz, 3 H), 1.02 (d, J=6.6 Hz, 3 H), 1.28-1.40 (m, 1 H), 1.59-1.69 (m, 1 H), 2.56-2.75 (m, 5 H), 3.48-3.67 (m, 4 H), 3.77 (s, 3 H), 6.35 (s, 1 H), 6.47 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-feae7e7919764cf38155c7e7562395e0 |
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| Source note | uspto-grants-2011_07 |
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