HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299028Generated: October 29, 2026
Methyl(2-pyridylmethyl)amine → HCID 57050861, compound
https://huagongshe.com/reaction/2299028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl(2-pyridylmethyl)amine | HCID 88757 | — |
| Reactant | HCID 57232508 | HCID 57232508 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 57050861 | HCID 57050861 | 22% |
Reaction Steps
N-[(5S)-3-(3-fluoro-4-(4-(1-benzotriazolyloxy)carbonylimidazol-1-yl)phenyl)-2-oxooxazolidin-5-ylmethyl]acetamide (prepared as detailed for Exarnples 49-80; 243 mg, 0.5 mM) dissolved in DMF (4 ml) was treated with 2-(N-methylaminomethyl)pyridine (68 mg, 0.55mM). The mixture was stirred under nitrogen, and heated to 55° for 18 hours. After cooling, the mixture was diluted with saturated sodium bicarbonate solution (20 ml), extracted with ethyl acetate (2×10 ml), the extract washed with water and dried over magnesium sulfate. After evaporation the residue was dissolved in dichloromethane and the solution chromatographed on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 20% methanol in dichloromethane. Relevant fractions were combined and evaporated to give title product (52 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495551B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-eb96cebdf758486fb541f375ddd1ebd8 |
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| Source note | uspto-grants-2002_12 |
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