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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264590Generated: November 1, 2026

1-(3-Aminopropyl)-4-methylpiperazine → HCID 59596407, compound

https://huagongshe.com/reaction/2264590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Aminopropyl)-4-methylpiperazineHCID 78328—
Reactant2-NaphthylalanineHCID 185915—
ReactantHCID 58659388HCID 58659388—
SolventIsopropanolHCID 3776—
ProductHCID 59596407HCID 59596407—

Reaction Steps

304 ring (0.70 mMol) of 5-(6-Chloro-pyrimidin-4-yloxy)-2,3-dihydro-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide (WO 03/099771; Stage 163), 477 μl (2.8 mMol) 1-(3-aminopropyl)-4-methyl-piperazine and a trace of Nal are heated in 10 ml isopropanol for 22 h at 50° C. Then the mixture is concentrated partially in vacuo. The residue is dissolved in EtOAc and NaHCO3 and the aqueous layer extracted twice with EtOAc. The organic layers are washed twice with water and brine, dried (Na2SO4) and concentrated. Column chromatography (SiO2; CH2Cl2/MeOH/NH3conc. 9:1:0→90:10:1) gives the title compound: m.p.: 163° C.; MS: [M+1]+=556; TLC(CH2Cl2/MeOH/NH3conc. 90:10:2): Rf=0.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855215B2
Source datasetuspto-grants-2010_12
ORD IDord-af3506b3e54442b19c7c990ba13338e2
Source noteuspto-grants-2010_12