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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028937Generated: November 1, 2026

Trifluoroacetic acid → (2-(2-Amino-3-morpholinoquinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

https://huagongshe.com/reaction/1028937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(2-(2-(4-Methoxybenzylamino)-3-morpholinoquinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanoneHCID 71253303—
Product(2-(2-Amino-3-morpholinoquinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanoneHCID 53328455—

Reaction Steps

A solution of (2-(2-(4-methoxybenzylamino)-3-morpholinoquinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone (30 mg, 0.056 mmol) and TFA (2 mL) was heated at 90° C. After 3 h, the reaction mixture was concentrated in vacuo, diluted with DCM and concentrated again. The crude product was dissolved in MeOH and filtered through an SCX (1 g) column then eluted with a 2M ammonia methanol solution to release the product. This filtrate was concentrated in vacuo to give a light orange solid that was washed with ether and decanted to remove most of the remaining starting material. The remaining solid was dissolved in DCM and purified by preparative thin layer chromatography (5×20 cm, 1000 um, 10% MeOH:DCM) to give (2-(2-amino-3-morpholinoquinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone as a white solid. MS (ESI, pos. ion) m/z: 417 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-2f90e7cb395a4f25b5c3a7d8accb77da
Source noteuspto-grants-2014_05