HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480094Generated: October 31, 2026
Acetic Acid → 6-(Methanesulfonyl)pyridin-3-amine
https://huagongshe.com/reaction/480094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(methylsulfonyl)-5-nitropyridine | HCID 1211552 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-(Methanesulfonyl)pyridin-3-amine | HCID 20038977 | 70.5% |
Reaction Steps
3-Nitro-6-(methylsulfonyl)pyridine (10 g, 49.5 mmol) was suspended in water (200 mL). Iron powder (5.0 g, 89.3 mmol) and acetic acid (0.5 mL) were added to the above mixture. The mixture, which resulted, was heated to reflux for 2 h. The reaction was monitored by TLC (EtOAc/hexane, 1/1). The reaction mixture was then cooled to rt and a saturated solution of NaHCO3 (100 mL) was added to the mixture. Ethyl acetate (200 mL) was added to the above mixture and the mixture which resulted was stirred at rt for 30 min. The mixture was filtered through celite and the organic layer was collectd. The aqueous layer was extracted with ethyl acetate (200 mL×3). The organic extractions were combined and dried (NaSO4). The solvent was removed under reduced pressure to provide the 3-amino-6-(methylsulfonyl)pyridine (6 g, 70.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649636B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-feb5a82fa893427bb914bfbfdbdfdb51 |
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| Source note | uspto-grants-2003_11 |
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