HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060994Generated: November 1, 2026
HCID 59239012, compound → HCID 59239000, compound
https://huagongshe.com/reaction/2060994
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59239012 | HCID 59239012 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59239000 | HCID 59239000 | — |
Reaction Steps
A mixture of 3-(5,7-dihydroindolo[2,3-b]carbazol-6-yl)-N,N-dimethylprop-2-yn-1-amine (30 mg, 0.08891 mmol), 10% Pd/C (10 mg, 0.0094 mmol) and methanol (20 mL) in a 250-mL hydrogenation bottle was filled with H2 and then degassed via house vacuum. This process was repeated three times. The reaction mixture was shaken at room temperature under H2 (30 psi) for 12 hours. The reaction solution was filtered through celite, and concentrated. The residue was subjected to flash chromatography to provide 3-(5,7-dihydroindolo[2,3-b]carbazol-6-yl)-N,N-dimethylpropan-1-amine. (10.2 mg, 34%). 1H-NMR (400 MHz, DMSO-d6) δ ppm 11.06 (s, 2H), 8.64 (s, 1H), 8.12 (d, J=7.6 Hz, 2H), 7.46 (d, J=8.0 Hz, 2H), 7.34-7.27 (m, 2H), 7.17-7.08 (m, 2H), 3.18 (t, J=7.4 Hz, 2H), 2.31 (t, J=7.2 Hz, 2H), 1.96-1.85 (m, 2H); MS (ESI) m/z 340.3 (M−H)−; MS (ESI) m/z 342.1 (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-857fab32697a441f8b7906c0777b3666 |
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| Source note | uspto-grants-2012_10 |
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