Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397769Generated: November 1, 2026

Dimethylformamide → 3-(Azidomethyl)-2-(3-fluorophenyl)-8-methoxyquinoline

https://huagongshe.com/reaction/1397769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium AzideHCID 33557—
Reactant3-(Chloromethyl)-2-(3-fluorophenyl)-8-methoxyquinoline hydrochlorideHCID 68944568—
Product3-(Azidomethyl)-2-(3-fluorophenyl)-8-methoxyquinolineHCID 86670072—

Reaction Steps

To a stirring solution of 3-(chloromethyl)-2-(3-fluorophenyl)-8-methoxyquinoline hydrochloride (0.9601 g, 2.839 mmol) in DMF (14.19 mL, 2.839 mmol) was added sodium azide (0.3691 g, 5.678 mmol) at room temperature and the mixture was stirred at room temperature After 1 h, the mixture was partitioned between EtOAc (100 mL) and H2O (100 mL). The organic layer was washed with brine (100 mL×1), dried over Na2SO4, filtered, and concentrated under reduced pressure to give 3-(azidomethyl)-2-(3-fluorophenyl)-8-methoxyquinoline as a yellow solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 8.48 (1 H, s), 7.54-7.62 (3 H, m), 7.43-7.49 (2 H, m), 7.32-7.39 (1 H, m), 7.21-7.28 (1 H, m), 4.68 (2 H, s), 3.97 (3 H, s); LC-MS (ESI) m/z 309.1 [M+H]+. The yellow solid was carried on crude without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901135B2
Source datasetuspto-grants-2014_12
ORD IDord-517d06726d784d8985f9071aa6c8fd4c
Source noteuspto-grants-2014_12