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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799475Generated: October 31, 2026

Trimethylsilyldiazomethane → HCID 59139878, compound

https://huagongshe.com/reaction/1799475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 68699892HCID 68699892—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59139878HCID 5913987843%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344138B2
Source datasetuspto-grants-2013_01
ORD IDord-0befee303bb446cebc9205a373a706aa
Source noteuspto-grants-2013_01