HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711080Generated: October 31, 2026
Dimethylformamide dimethyl acetal → 6-bromo-N-methylisoquinolin-3-amine
https://huagongshe.com/reaction/711080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6-Bromoisoquinolin-3-Amine | HCID 45789831 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-bromo-N-methylisoquinolin-3-amine | HCID 67491551 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181252B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-83b2ab9674e343548664875bcf506814 |
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| Source note | uspto-grants-2015_11 |
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