Yield:-

Reaction Conditions:

in ethyl acetate;trichlorophosphate;

Steps:

3 Step 3:

Step 3:
Preparation of 1-chloro-4-cyclopropylisoquinoline
A solution of 4-cyclopropylisoquinoline-2-oxide (0.3 g, 1.620 mmol) in POCl₃ (15 ml) was refluxed for overnight.
The solvent was evaporated under reduced pressure and the residue was diluted with cold water.
The aqueous solution was basified by solid sodium carbonate and extracted with ethyl acetate.
The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to get crude compound.
The crude compound was purified by silica gel chromatography (10% ethyl acetate in pet ether) to get the desired compound (0.02 g, 5.76%) as oil. ¹H NMR (400 MHz, CDCl₃): δ ppm 8.37-8.35 (d, J=8 Hz, 2H), 8.08 (s, 1H), 7.81 (t, J=8 Hz, 1H), 7.70 (t, J=4 Hz, 1H), 2.18 (m, 1H), 1.11 (t, J=4 Hz, 2H), 0.80 (t, J=8 Hz, 2H); MS: MS m/z 204.28 (M⁺+1).

References:

US2013/115190,2013,A1 Location in patent:Page/Page column