HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445611Generated: October 31, 2026
Methyl iodide → N-(5-Bromo-2-methoxy-pyridin-3-yl)-N-methyl-acetamide
https://huagongshe.com/reaction/445611
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(5-bromo-2-methoxypyridin-3-yl)acetamide | HCID 59619883 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5-Bromo-2-methoxy-pyridin-3-yl)-N-methyl-acetamide | HCID 59619892 | — |
Reaction Steps
To N-(5-bromo-2-methoxy-pyridin-3-yl)-acetamide (Stage 62.1.3, 100 mg, 0.408 mmol) DMF (1 ml) was added NaH 55% in oil (19.6 mg, 0.45 mmol). The reaction mixture was stirred for 10 min at rt then was added MeI (0.031 ml, 0.49 mmol). The reaction mixture was stirred for 1 h at rt then quenched with brine and extracted with EtOAc (2×). The organic layers are washed with brine (3×), dried over Na2SO4, filtered and evaporated. The crude product was purified by Prep.HPLC. The fractions containing the product were collected together and basified with NaHCO3, before being concentrated and extracted with EtOAc (3×). The organic layers were dried over Na2SO4, filtered and evaporated to dryness to give the title compound as an off-white solid (HPLC: tR 2.75 min (Method A); M+H=259, 261 MS-ES).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476294B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-81934f1f76014f1a923ae8b1fb27f761 |
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| Source note | uspto-grants-2013_07 |
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