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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966916Generated: October 26, 2026

Trifluoroacetic acid → 4-Aminoisoquinoline-1-carbonitrile

https://huagongshe.com/reaction/966916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(2,4-Dimethoxy-benzylamino)-isoquinoline-1-carbonitrileHCID 21875414—
Product4-Aminoisoquinoline-1-carbonitrileHCID 2187527292%

Reaction Steps

Compound 470C (50 mg, 0.16 mmol) was treated with trifluoroacetic acid (0.5 mL) for 1 h. The highly colored mixture was partitioned between ethyl acetate (30 mL) and 1N NaOH (30 mL). After washing with brine (15 mL), the organic layer was dried over magnesium sulfate and concentrated in vacuo to afford 24 mg (92%) of compound 470D as a yellow solid. HPLC: 99% at 1.09 min (retention time) (Phenomenex C-18, 5 micron column, 4.6×30 mm, eluting with 10-90% aqueous methanol over 2 min containing 0.1% TFA, 4 mL/min, monitoring at 254 nm). MS (ES+): m/z 170.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953679B2
Source datasetuspto-grants-2005_10
ORD IDord-124328f5d1014e3cac462c6cf1639773
Source noteuspto-grants-2005_10