HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275017Generated: October 25, 2026
Triethylamine → N-[4-Chloro-3-(4-methylpiperazin-1-yl)phenyl]-N'-[4-(pyridin-4-yl)naphth-1-yl]urea
https://huagongshe.com/reaction/1275017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 4-(Pyridin-4-yl)naphth-1-ylamine | HCID 10857012 | — |
| Reactant | 4-Chloro-3-(4-methylpiperazin-1-yl)aniline | HCID 18180073 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-Chloro-3-(4-methylpiperazin-1-yl)phenyl]-N'-[4-(pyridin-4-yl)naphth-1-yl]urea | HCID 22118919 | — |
Reaction Steps
To a stirred solution of triphosgene (39 mg, 0.13 mmole) in dichloromethane (10 ml) was added a solution of 4-(pyridin-4-yl)naphth-1-ylamine (D1, 82 mg, 0.37 mmole) and triethylamine (0.05 ml, 0.37 mmole) dropwise over 30 minutes. When the addition was complete the mixture was stirred at room temperature for 15 minutes, then a solution of 4-chloro-3-(4-methylpiperazin-1-yl)aniline (100 mg, 0.44 mmole, EP0533268A1) in dichloromethane (10 ml) was added over 5 minutes. After 18 h, the mixture was washed with 10% aqueous sodium carbonate solution and water, dried (Na2SO4) and evaporated to dryness. The residue was purified by column chromatography on silica gel eluting with 10% methanol/dichloromethane and the title compound was obtained as a white solid on trituration with ether (47 mg, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06159979 |
|---|
| Source dataset | uspto-grants-2000_12 |
|---|
| ORD ID | ord-58d818f6374b4e928a506fea67f2417a |
|---|
| Source note | uspto-grants-2000_12 |
|---|