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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723683Generated: October 26, 2026

Trifluoroacetic acid → 4-Aminoisoquinoline-1-carbonitrile

https://huagongshe.com/reaction/723683

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 numberUS07141578B2
Source datasetuspto-grants-2006_11
ORD IDord-8bd82921c54b4f14be08731a1b47a9cd
Source noteuspto-grants-2006_11