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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110443Generated: October 27, 2026

Trifluoroacetic acid → 4-Aminoisoquinoline-1-carbonitrile

https://huagongshe.com/reaction/2110443

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 numberUS07517904B2
Source datasetuspto-grants-2009_04
ORD IDord-2596a63c23a84c839ddb3d6a0833cdd0
Source noteuspto-grants-2009_04