HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060978Generated: November 1, 2026
HCID 59238895, compound → HCID 59239005, compound
https://huagongshe.com/reaction/2060978
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59238895 | HCID 59238895 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59239005 | HCID 59239005 | 64% |
Reaction Steps
A mixture of 2-(2,10-dibromo-5,7-dihydroindolo[2,3-b]carbazol-6-yloxy)-N,N-diethylethanamine (133.0 mg, 0.2513 mmol) and 10% Pd/C (0.05 equivalent) in DMF (8 mL) in a hydrogenation flask was filled with H2 and then evacuated with house vacuum for three times, and then filled with H2 (30˜40 psi). The reaction was stirred at room temperature overnight. When TLC and MS showed the reaction was complete, the DMF solvent was removed under vacuum pump. The residue was dissolved in methanol and filtered through celite. The crude product was purified by flash chromatography to provide the desired product 2-(5,7-dihydroindolo[2,3-b]carbazol-6-yloxy)-N,N-diethylethanamine (59.3 mg, 64%). 1H-NMR (400 MHz, CD3OD) δ ppm 8.47 (s, 1H), 8.09 (d, J=7.6 Hz, 2H), 7.49 (d, J=8.0 Hz, 2H), 7.33 (t, J=8.0 Hz, 2H), 7.16 (t, J=7.6 Hz, 2H), 4.57 (t, J=5.0 Hz, 2H), 3.79 (t, J=5.0 Hz, 2H), 3.49 (q, J=7.6 Hz, 4H), 1.45 (t, J=7.6 Hz, 6H); MS (ESI) m/z 370.3 (M−H)−; MS (ESI) m/z 372.1 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278341B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-68b6e08d19614c37af916cdf08083623 |
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| Source note | uspto-grants-2012_10 |
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