HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401309Generated: November 1, 2026
2-Methoxyethylamine → 6-Bromo-N-(2-methoxyethyl)-3-pyridinemethanamine
https://huagongshe.com/reaction/1401309
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6-Bromo-3-pyridinecarboxaldehyde | HCID 11769234 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-N-(2-methoxyethyl)-3-pyridinemethanamine | HCID 57919478 | 45% |
Reaction Steps
To a solution of 6-bromonicotinaldehyde (7) (5 g, 26.9 mmol) in DCM (40 μL) was added 2-methoxyethylamine (8) (2.80 mL, 32.3 mmol). After 10 min, sodium triacetoxyborohydride (7.98 g, 37.6 mmol) was added to the mixture and the mixture was stirred at r.t. for 17 h. Additional amounts of DCM (100 mL), water (50 mL) and NH4Cl (50 mL) were added to the reaction mixture, which turned into a biphasic system. The organic phase was collected and the aqueous layer was extracted with DCM (3×100 μL). The combined organic solution were washed with brine, dried over anhydrous MgSO4 and concentrated under reduce pressure. The residue was purified by flash column chromatography (eluent a gradient DCM/MeOH from 98/2 to 95/5), to afford intermediate 9 (2.958 g, 45% yield) as a brown oil. MS (m/z): 245.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907091B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-32a7270aa3d4438383a62c9b7ab9ae37 |
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| Source note | uspto-grants-2014_12 |
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