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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435171Generated: November 2, 2026

4-[4-(Propan-2-yl)piperazin-1-yl]aniline → [4-Amino-2-[4-(4-isopropyl-piperazin-1-yl)-phenylamino]-pyrimidin-5-yl]-(2-methoxy-phenyl)-methanone

https://huagongshe.com/reaction/1435171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[4-(Propan-2-yl)piperazin-1-yl]anilineHCID 9161545—
Reactant(4-Amino-2-ethanesulfonylpyrimidin-5-yl)-(2-methoxyphenyl)-methanoneHCID 11961965—
SolventIsopropanolHCID 3776—
Product[4-Amino-2-[4-(4-isopropyl-piperazin-1-yl)-phenylamino]-pyrimidin-5-yl]-(2-methoxy-phenyl)-methanoneHCID 2107046942.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of (4-amino-2-ethanesulfonylpyrimidin-5-yl)-(2-methoxyphenyl)-methanone (26.6 mg, 0.0828 mmol, Example 6) and 4-(4-isopropylpiperazin-1-yl)phenylamine (19.5 mg, 0.0889 mmol) in isopropanol (2.5 mL) was placed in a sealed tube and heated at 110° C. under microwave conditions for 1 hour. The resulting mixture was concentrated and the crude product was purified on silica gel with 95:5 of dichloromethane/methanol to give [4-amino-2-[4-(4-isopropyl-piperazin-1-yl)-phenylamino]-pyrimidin-5-yl]-(2-methoxy-phenyl)-methanone as a light yellow solid (15.6 mg, 42% yield). HRMS, observed: 447.2507; Calcd for (M+H)+: 447.2503.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615634B2
Source datasetuspto-grants-2009_11
ORD IDord-47d97cbde1d5456d86f14c22a94d00d5
Source noteuspto-grants-2009_11