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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-bis(3-aminopropyl)methylamine | HCID 7777 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl ester | HCID 20829786 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06946472B2 |
|---|
| Source dataset | uspto-grants-2005_09 |
|---|
| ORD ID | ord-47ebe698c6114793aab8c2c5be8b4eb9 |
|---|
| Source note | uspto-grants-2005_09 |
|---|