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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451486Generated: 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/1451486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BOC-ethylenediamineHCID 187201—
Reactant2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-(p-toluenesulfonyl oxy)isoquino[8,7,6cd]indazole-6(2H)-oneHCID 10506481—
SolventPyridineHCID 1049—
Product2-[2-(N-tert-butoxycarbonylamino)ethyl]-5-[[2-(N-tert-butoxycarbonylamino)ethyl]amino]isoquino[8,7,6-cd]indazole-6(2H)-oneHCID 10815879—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604246
Source datasetuspto-grants-1997_02
ORD IDord-1a889f0b0701441e9b13915a5f554767
Source noteuspto-grants-1997_02