HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352373Generated: October 30, 2026
Triethylamine → cis-5-Methoxy-1-[4-(6-methylpyridin-2-yl)-1-naphthylaminocarbonyl]-6-(3,4,5-trimethylpiperazin-1-yl)indoline
https://huagongshe.com/reaction/352373
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 4-(6-Methylpyridin-2-yl)-1-naphthoic acid | HCID 22711846 | — |
| Reactant | cis-5-Methoxy-6-(3,4,5-trimethylpiperazin-1-yl)indoline | HCID 69836129 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cis-5-Methoxy-1-[4-(6-methylpyridin-2-yl)-1-naphthylaminocarbonyl]-6-(3,4,5-trimethylpiperazin-1-yl)indoline | HCID 69836264 | 52.3% |
Reaction Steps
A stirred mixture of D13 (87 mg, 0.33 mmole), triethylamine (40 mg, 0.40 mmole) and diphenylphosphoryl azide (96 mg, 0.35 mmole) in toluene was heated at reflux under argon for 0.5 h, then allowed to cool to room temperature and treated with a solution of D3 (70 mg, 0.25 mmole) in DCM (10 ml). The mixture was stirred at room temperature for 4 h, then treated with polystyrene bound trisamine (80 mg of 3.6 mmole/g) and polystyrene bound methylisocyanate (60 mg of 1.2 mmole/g) and stirred at room temperature for 70 h, then filtered through Kieselguhr. The filtrate was washed with 10% Na2CO3 solution, dried (Na2SO4), concentrated under vacuum and purified by chromatography on basic alumina eluting with EtOAc, followed by trituration with Et2O to afford the title compound as a yellow solid (70 mg, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747030B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-9c15c80b24134ffbb31e44ae69f45395 |
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| Source note | uspto-grants-2004_06 |
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