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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244067Generated: October 31, 2026

Water → 1-Amino-4-bromo-6-fluoro-isoquinoline

https://huagongshe.com/reaction/2244067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Fluoroisoquinolin-1-amineHCID 25059437—
SolventChloroformHCID 6212—
Product1-Amino-4-bromo-6-fluoro-isoquinolineHCID 2505943865%

Reaction Steps

To a solution of 1-amino-6-fluoro-isoquinoline (0.41 g, 2.53 mmol) in CHCl3 (25 mL) is added NBS (0.45 g, 2.53 mmol), and the reaction mixture is stirred RT for 1.5 h. The reaction mixture is treated with water (10 mL). The aqueous phase is extracted with CH2Cl2 (2×). The combined organic layers are washed with brine, and dried over MgSO4. The solvent is evaporated and the residue is dried under vacuum. Purification of the crude material using a Biotage column (10-40% MeOH/CH2Cl2) afforded 0.395 g (65%) of 1-amino-4-bromo-6-fluoro-isoquinoline. LC/MS m/z=242 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678803B2
Source datasetuspto-grants-2010_03
ORD IDord-3fc3988f8edd4947aa7422e84c3e3061
Source noteuspto-grants-2010_03