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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778105Generated: November 4, 2026

Trifluoroacetic acid → HCID 118036501, compound

https://huagongshe.com/reaction/1778105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 118036691HCID 118036691—
SolventDichloromethaneHCID 6344—
ProductHCID 118036501HCID 118036501—

Reaction Steps

A solution of N-(4-((2-(tert-butoxy)ethyl)amino)-5-cyanopyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide (Example 196, 1.11 g, 2.02 mmol) in DCM (10 ml) was treated with CF3CO2H (1.56 ml, 20.23 mmol). The reaction mixture was stirred for 48 h. The reaction was quenched by addition of saturated Na2CO3 solution. The reaction mixture was stirred for 16 h. The aqueous was extracted with DCM (×2) and the combined organic extracts were concentrated under reduced pressure. The solid was dissolved in a minimum amount of DCM with a drop of MeOH, then Et2O was added to give a precipitate which was filtered. The solid was triturated with Et2O and filtered to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-363ff95638e94de28742a773721a01f8
Source noteuspto-grants-2016_02