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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496741Generated: October 26, 2026

N,N-bis(3-aminopropyl)methylamine → 6-(3-{methyl-[3-(7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-ylamino)-propyl]-amino}-propylamino)-5,9-diaza-benzo[c]fluoren-7-one

https://huagongshe.com/reaction/496741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-bis(3-aminopropyl)methylamineHCID 7777—
ReactantPotassium CarbonateHCID 11430—
Reactanttoluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl esterHCID 20829786—
SolventDichloromethaneHCID 6344—
Product6-(3-{methyl-[3-(7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-ylamino)-propyl]-amino}-propylamino)-5,9-diaza-benzo[c]fluoren-7-oneHCID 10393889—

Reaction Steps

A mixture of toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl ester (Reference Example 6c-2) (90 mg) and N1-(3-amino-propyl)-N1-methyl-propane-1,3-diamine (WAKO PURE CHEMICAL: 15 mg) and potassium carbonate (37 mg) was suspended in dichloromethane (10 ml) and heated at reflux temperature for five days under nitrogen. The mixture was roughly purified by short silica gel column chromatography developed by dichloromethane-methanol=100:1 and dichloromethane-methanol=1:1. The fractions that contained the desired product were combined and evaporated to dryness and purified again by silica gel thin layer chromatography developed by dichloromethane-methanol-ammonia water=90:10:1. The desired compound was obtained as a dark reddish powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946472B2
Source datasetuspto-grants-2005_09
ORD IDord-47ebe698c6114793aab8c2c5be8b4eb9
Source noteuspto-grants-2005_09