HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537136Generated: October 28, 2026
7-Bromo-1-Chloroisoquinoline → 7-Bromo-1-methoxyisoquinoline
https://huagongshe.com/reaction/537136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Bromo-1-Chloroisoquinoline | HCID 6502024 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Bromo-1-methoxyisoquinoline | HCID 67491611 | 93% |
Reaction Steps
7-Bromo-1-chloroisoquinoline (570 mg, 2.4 mmol) was combined with methanol (10 mL) and sodium methoxide (25 wt % in methanol, 1.5 mL, 24 mmol) in a microwave vial. The vial was sealed and heated to 130° C. for 3 hours in a microwave. The reaction was concentrated. The crude residue was taken up in ethyl acetate and washed with water and saturated aqueous sodium bicarbonate. The aqueous layer was extracted two times with hot ethyl acetate. The combined organics were dried over sodium sulfate, filtered, and concentrated to give the title compound (520 mg, 93%). +ESI (M+H+1) 240.0; 1H NMR (400 MHz, DMSO-d6, δ): 8.25-8.28 (m, 1H), 8.04 (d, J=5.9 Hz, 1H), 7.86-7.89 (m, 2H), 7.40 (dd, J=6.0, 0.9 Hz, 1H), 4.03 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859773B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-dea21a31665d4ae1a139ad5a651f73d6 |
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| Source note | uspto-grants-2014_10 |
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