HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583180Generated: October 25, 2026
Ammonium Hydroxide → 6-Bromo-5-methoxypyridin-2-amine
https://huagongshe.com/reaction/583180
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 2-Bromo-3-methoxy-6-nitropyridine | HCID 12692873 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 6-Bromo-5-methoxypyridin-2-amine | HCID 12758209 | 50% |
Reaction Steps
2-Bromo-3-methoxy-6-nitropyridine (470 mg, 2.0 mmol) was added to 8 mL (3:1 water: ethanol) and 2 mL of 30% ammonium hydroxide. Added 350 mg (2 mmol) of sodium hydrosulfite (Na2SsO4) and heated to 60° C. After 30 min, no starting material was seen. Added 50 mL of water and extracted the product with methylene chloride (2×25 mL). Dried over MgSO4, filtered and reduced the volume. Flash chromatography (75/25 hexane/ethyl acetate) recovered 200 mg of product (50% yield). 1H NMR (CDCl3, 200 MHz) δ 7.06 (d, 1H, 10 Hz), 6.41 (d, 1H, J=10 Hz), 3.8 (s, 3H) ppm
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929094 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-4ca2a55c909848c791a3cd71e19db04a |
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| Source note | uspto-grants-1999_07 |
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