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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005608Generated: October 29, 2026

Trimethylsilyldiazomethane → HCID 18791582, compound

https://huagongshe.com/reaction/1005608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 18791518HCID 18791518—
SolventMethanolHCID 887—
ProductHCID 18791582HCID 18791582—

Reaction Steps

To a solution of 4-[2-[(3-tert-butoxycarbonylaminoprop-1-yl)oxy]benzoyl]amino-3-carboxymethoxy-N-methyl-N-[2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]-4-methylphenyl]benzamide (128 mg) in methanol (5 ml) was added dropwise trimethylsilyldiazomethane (5 ml, 2.0M n-hexane solution) and stirred at ambient temperature for 30 minutes. The solution was concentrated in vacuo and the residue was purified by preparative thin layer silica gel chromatography (chloroform:methanol:28% aqueous ammonia solution, 50:5:1) to give 4-[2-[(3-tert-butoxycarbonylaminoprop-1-yl)oxy]benzoyl]amino-3-methoxycarbonylmethoxy-N-methyl-N-[2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]-4-methylphenyl]benzamide (85 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054457
Source datasetuspto-grants-2000_04
ORD IDord-82302aecb8fe4f6c80207d1d1d9439dd
Source noteuspto-grants-2000_04