Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060978Generated: November 1, 2026

HCID 59238895, compound → HCID 59239005, compound

https://huagongshe.com/reaction/2060978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59238895HCID 59238895—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
ProductHCID 59239005HCID 5923900564%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278341B2
Source datasetuspto-grants-2012_10
ORD IDord-68b6e08d19614c37af916cdf08083623
Source noteuspto-grants-2012_10