HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799475Generated: October 31, 2026
Trimethylsilyldiazomethane → HCID 59139878, compound
https://huagongshe.com/reaction/1799475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | HCID 68699892 | HCID 68699892 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59139878 | HCID 59139878 | 43% |
Reaction Steps
According to Scheme 7 Step 5: To a solution of 2-(3-acetamidophenyl)-4-(4-chlorobenzyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylic acid 11(D) (80 mg, 0.19 mmol) in MeOH (3 mL) was added dropwise at 0° C. a solution of trimethylsilyldiazomethane 2M (1.3 mL, 2.70 mmol). The mixture was stirred at room temperature for 18 h. The mixture was diluted with 100 mL of a saturated solution of NaHCO3 and the aqueous layer was extracted twice with 100 mL of DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure to afford a yellow solid. The crude solid was purified by flash chromatography with silica gel (AIT Flashmart prepacked column 7 g SiO2) using CH2Cl2/MeOH 98/2 as eluant to afford a yellow solid. The solid was further triturated with diisopropylether and filtered to afford methyl 4-(4-chlorobenzyl)-2-(3-acetamidophenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxylate (35 mg, 42%) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344138B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-0befee303bb446cebc9205a373a706aa |
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| Source note | uspto-grants-2013_01 |
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