HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440365Generated: October 27, 2026
N-BOC-ethylenediamine → 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(N-tert-butoxycarbonylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one
https://huagongshe.com/reaction/440365
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| 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-(N-tert-butoxycarbonylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-one | HCID 10815879 | — |
Reaction Steps
A suspension of 2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6(2H)-one of Example 3 (0.535 g) and N-(tert-butoxycarbonyl)ethylenediamine (prepared according to Synt. Comm., 20, 2559, (1990); 1.12 g) in dry pyridine (5.35 mL) is heated at 80° C. The dark solution obtained is held at this temperature for 5 hours, then it is concentrated to dryness and partitioned between brine (30 mL) and ethyl acetate (2×25 mL). The orange-red solid insoluble in the biphasic mixture is separated by suction filtration and dried at 40° C. under vacuum (0.43 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05519029 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-dbe43612d75842b48ee3ab301a161cd7 |
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| Source note | uspto-grants-1996_05 |
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