HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451484Generated: October 27, 2026
N,N-Dimethylethylenediamine → 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one
https://huagongshe.com/reaction/1451484
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | 2-methyl-5-(p-toluenesulfonyloxy)isoquino [8,7,6-cd]indazole-6(2H)-one | HCID 15337874 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one | HCID 15337875 | — |
Reaction Steps
A 1M solution of N,N-dimethylethylenediamine in pyridine (0.10 mL) is added to a stirred suspension of 2-methyl-5-(p-toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6(2H)-one (0.02 g) in dry pyridine (2 mL). After stirring at room temperature for one hour the reaction mixture is heated at 70° C. for 13 hours while additional amounts of N,N-dimethylethylenediamine solution (0.1; 0.05; 0.05 mL) are added after 2, 4 and 11 hours respectively. Pyridine and excess N,N-dimethylethylenediamine are removed by distillation at reduced pressure and the obtained residue is partitioned between CH2Cl2 (50 mL) and brine (10 mL) to which NaHCO3 saturated solution is added (1 mL). The organic solution is dried over anhydrous Na2SO4 and the solvent removed by distillation. The orange residue obtained is purified by silica-gel column chromatography (eluant: CHCl3 /MeOH 95/5 (30 mL) followed by CHCl3 /MeOH/NH4OH 90/15/0.5 (50 mL) to give 2-methyl-5-[[2-(dimethylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one (0.011 g) as a reddish orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604246 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-bc6ea1ed3a0a4c91af382eb81d551703 |
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| Source note | uspto-grants-1997_02 |
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