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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537157Generated: October 30, 2026

Dimethylformamide dimethyl acetal → 6-bromo-N-methylisoquinolin-3-amine

https://huagongshe.com/reaction/537157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-Bromoisoquinolin-3-AmineHCID 45789831—
SolventDimethylformamideHCID 6228—
Product6-bromo-N-methylisoquinolin-3-amineHCID 6749155143%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 6-bromoisoquinolin-3-amine (50.0 mg, 2.6 mmol) in N,N-dimethylformamide (10 mL) was added N,N-dimethylformamide dimethylacetal (2 mL). The reaction vessel was sealed and heated in a Biotage Smith Synthesizer microwave to 110° C. for 20 minutes. Sodium triacetoxyborohydride (59 mg, 0.28 mmol) was then added to the reaction mixture. The vial was resealed and heated again to 110° C. on a Biotage Smith Synthesizer microwave for 10 minutes. The reaction was concentrated. The residue was dissolved in ethyl acetate (50 mL) and washed with brine (2×20 mL). The organics were dried over sodium sulfate, filtered, and concentrated. Purification by flash column chromatography gave the title compound (23 mg, 43%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 8.76 (s, 1H), 7.74 (s, 1H), 7.61 (d, 1H), 7.28 (d, 1H), 6.40 (s, 1H), 5.09-5.07 (m, 1H), 2.97 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859773B2
Source datasetuspto-grants-2014_10
ORD IDord-62757f9dbbc84a259faa25cf267a7d40
Source noteuspto-grants-2014_10