HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441935Generated: November 1, 2026
HCID 11568302, compound → HCID 11551968, compound
https://huagongshe.com/reaction/1441935
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 11568302 | HCID 11568302 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11551968 | HCID 11551968 | — |
Reaction Steps
Nitrogen flushed mixture of 4-bromo-phenyl-carbamic acid 1-benzyl-1,2,3,4-tetrahydro-quinolin-6-yl ester (0.655 g., 1.5 mmol) and 5% Pd—C (0.06 g.) in absolute ethanol (20 ml) was shaken in a par apparatus at room temperature (40° C.) under 50 psi pressure of hydrogen for 5 hours. Then Pd—C was discarded through filtration. The reaction mixture was concentrated under reduced pressure and the residue was washed with dichloromethane (2×3ml) to give 2f; yield: 0.48 g. (92.3%), m.p: 198° C., C16H15BrN2O2; 1H NMR δ ppm (DMSO): 1.82-2.00 (bs, 2H), 2.76 (t, 2H), 3.27 (t, 2H), 7.01-7.08 (m, 3H), 7.25-7.39 (m, 4H), 10.14 (s, 1H), IR vmax (KBr) (cm−1): 506, 608, 690, 749, 814, 884, 927, 1005, 1211, 1265, 1319, 1354, 1401, 1440, 1501, 1550, 1601, 1748, 1938, 2370, 2779, 2725, 2767, 2823, 2922, 3262, 3420, 3774.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655801B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-3337ad36a14549fba632efd3bd934c0a |
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| Source note | uspto-grants-2010_02 |
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