HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625980Generated: October 30, 2026
Stannous chloride dihydrate → 5-Bromo-2-methoxypyridin-3-amine
https://huagongshe.com/reaction/1625980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 5-Bromo-2-methoxy-3-nitropyridine | HCID 15645664 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-2-methoxypyridin-3-amine | HCID 44754869 | 58.7% |
Reaction Steps
To a solution of 5-bromo-2-(methyloxy)-3-nitropyridine (45 g, 193 mmol) in ethyl acetate (1 L) was added tin (II) chloride dihydrate (174 g, 772 mmol). The reaction mixture was heated at reflux for 4 h. LC/MS indicated some starting material remained, so added 20 mol % tin (II) chloride dihydrate and continued to heat at reflux. After 2 h, the reaction was allowed to cool to ambient temperature and concentrated in vacuo. The residue was treated with 2 N sodium hydroxide and the mixture stirred for 1 h. The mixture was then with methylene chloride (1 L), filtered through Celite, and washed with methylene chloride (500 mL). The layers were separated and the organics dried over magnesium sulfate and concentrated to give 5-bromo-2-(methyloxy)-3-pyridinamine (23 g, 113 mmol, 58.7% yield). The product was used crude in subsequent reactions. MS(ES)+ m/e 201.9, 203.9 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08785433B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-d065a902aea846a2a2df895301a3d68e |
|---|
| Source note | uspto-grants-2014_07 |
|---|