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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-(6-Methylpyridin-2-yl)-1-naphthoic acidHCID 22711846—
Reactantcis-5-Methoxy-6-(3,4,5-trimethylpiperazin-1-yl)indolineHCID 69836129—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Productcis-5-Methoxy-1-[4-(6-methylpyridin-2-yl)-1-naphthylaminocarbonyl]-6-(3,4,5-trimethylpiperazin-1-yl)indolineHCID 6983626452.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747030B1
Source datasetuspto-grants-2004_06
ORD IDord-9c15c80b24134ffbb31e44ae69f45395
Source noteuspto-grants-2004_06