HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451487Generated: October 26, 2026
N,N-Dimethylethylenediamine → 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(dimethylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one
https://huagongshe.com/reaction/1451487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyl oxy)isoquino[8,7,6cd]indazole-6(2H)-one | HCID 10506481 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(dimethylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one | HCID 10742198 | — |
Reaction Steps
A suspension of 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyloxy) isoquino[8,7,6-cd]indazole-6(2H)-one (0.056 g) and 2-(dimethylamino)ethylamine (0.080 mL) in dry pyridine (0.50 mL) is heated at 80° C. The dark solution obtained is held at this temperature for 1 hour, then it is left at room temperature overnight. The dark precipitate obtained is separated by suction and purified by column chromatography (SiO2 ; eluant ethyl acetate and then methylene chloride/methanol 9/0.5 v/v) to give 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(dimethylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one (0.024 g) as a red-orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05604246 |
|---|
| Source dataset | uspto-grants-1997_02 |
|---|
| ORD ID | ord-8780df86376645f2bc4d6707933be52d |
|---|
| Source note | uspto-grants-1997_02 |
|---|