HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069123Generated: November 2, 2026
Diisopropylethylamine → 2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamide
https://huagongshe.com/reaction/2069123
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methoxyacetyl chloride | HCID 96623 | — |
| Reactant | 4-(4-Nitrophenoxy)pyridin-2-amine | HCID 22936716 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamide | HCID 70921741 | 92.6% |
Reaction Steps
To a solution of 4-(4-nitrophenoxy)pyridin-2-amine [US Pat Appl 2008319188, Production Example 53] (0.60 g, 2.60 mmol) and DIPEA (0.680 μL, 3.89 mmol) in DCM (15.0 mL) under nitrogen at 0° C. was added 2-methoxyacetyl chloride (225 μL, 3.89 mmol) dropwise over 5 min. The reaction was maintained at RT for 16 hr and was quenched by the addition of a 1% solution of NH3 in MeOH (10 mL). The mixture was evaporated in vacuo and the residue was taken up into DCM (50 mL) and was washed with water (25 mL) and brine (25 mL), and then dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, EtOAc in DCM, 0-30%, gradient elution) to afford 2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamide as a white solid (0.73 g, 92%); Rt 1.88 min (Method 2); m/z 304 (M+H)+ (ES+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299074B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-3442da9e5af541859f8b47a776c7c0aa |
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| Source note | uspto-grants-2012_10 |
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