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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861674Generated: October 31, 2026

Sodium Azide → 5-(Azidomethyl)isoquinoline

https://huagongshe.com/reaction/1861674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant5-(Chloromethyl)isoquinolineHCID 12018694—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-(Azidomethyl)isoquinolineHCID 12018695—

Reaction Steps

To a solution of 0.0415 g (0.23 mmol) 16 in 3 mL DMF was added 0.0169 g (0.26 mmol) sodium azide. After a 3 h, an additional 0.0033g (0.05 mmol) portion of sodium azide was added. After 24 h at room temperature, the reaction mixture was diluted with 50 mL EtOAc and washed with 20 mL brine. The aqueous layer was extracted with 10 mL EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (10×175 mm silica gel, linear gradient 5-20% EtOAc:hexane) produced 17. 1H NMR (CDCl3, 400 MHz) δ 9.318 (s, 1H, ArH); 8.637 (d, 1H, J=6.10 Hz, ArH); 8.010 (d, 1H, J=7.94 Hz, ArH); 7.822 (d, 1H, J=6.10 Hz, ArH); 7.713 (d, 1H, J=7.02 Hz, ArH); 7.617 (dd, 1H, J=7.17, 8.09 Hz, ArH); 4.774 (s, 1H, ArH); MS (Electrospray): m/z 185.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534510B2
Source datasetuspto-grants-2003_03
ORD IDord-8532594578b346208285051fece14f70
Source noteuspto-grants-2003_03