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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406477Generated: October 29, 2026

Diisopropylethylamine → 2-(7-Chloroquinazolin-4-ylamino)-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanone

https://huagongshe.com/reaction/406477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,7-DichloroquinazolineHCID 241881—
Reactant2-Amino-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanoneHCID 59764695—
Solvent1-ButanolHCID 263—
Product2-(7-Chloroquinazolin-4-ylamino)-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanoneHCID 5976487258.9%

Reaction Steps

A solution of 2-amino-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanone (preparation #9) (0.108 g, 0.377 mmol), 4,7-dichloroquinazoline (0.075 g, 0.377 mmol) and DIEA (0.1 mL, 0.565 mmol) in n-butanol was heated in a microwave (CEM Explorer, maximum power 300 W) at about 120° C. for about 20 min. The solvent was removed in vacuo and the residue was purified by preparative RP-HPLC (20% to 50% acetonitrile/0.05M aqueous ammonium acetate, buffered to pH 4.5, over 30 min at 81 mL/min; λ=254 nm; Microsorb C18, 100 Å, 5 μm, 250×46 mm column) to yield 2-(7-chloroquinazolin-4-ylamino)-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanone (0.100 g, 0.222 mmol) as a yellow solid. RP-HPLC (Table 1, Method a) Rt 1.77 min; m/z: (M+H)+ 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754107B2
Source datasetuspto-grants-2014_06
ORD IDord-7545b19221ed4840be23e9bd27faa9de
Source noteuspto-grants-2014_06