HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624879Generated: October 29, 2026
Sodium Methoxide → N-(3-(4-(4-chlorobenzyl)-6-methoxy-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide
https://huagongshe.com/reaction/1624879
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-(3-(4-(4-chlorobenzyl)-6-bromo-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide | HCID 68702221 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-(4-(4-chlorobenzyl)-6-methoxy-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide | HCID 59139822 | 35% |
Reaction Steps
According to Scheme 2 Step 4: To a cooled solution of N-(3-(4-(4-chlorobenzyl)-6-bromo-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide 2(C) (80 mg, 0.18 mmol) in 0.5 mL of methanol (0.5 mL) at 0° C., was added a solution of sodium methoxide (2M) in Methanol (85 μL 0.18 mmol). After 1 h at 0° C. the reaction mixture was allowed to reach room temperature. After 1 h the reaction mixture was quenched with water and extracted with ethyl acetate (×3). The combined organic layers were washed successively with water, with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash chromatography, 5 g column, (Eluant: DCM/AcOEt/MeOH 80/18/2). 25 mg (35% yield) of N-(3-(4-(4-chlorobenzyl)-6-methoxy-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide were recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779129B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-fc0ada27827142c499ff0c2fc6c37454 |
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| Source note | uspto-grants-2014_07 |
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