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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897320Generated: October 30, 2026

Trimethylsilyldiazomethane → HCID 22346362, compound

https://huagongshe.com/reaction/897320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 22346269HCID 22346269—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 22346362HCID 22346362—

Reaction Steps

To a suspension of N-(4-fluorobenzyl)-8-hydroxy-5-(methylamino)-1,6-naphthyridine-7-carboxamide (2.65 g, 8.12 mmol) in methanol (50 mL) and CH2Cl2 (20 mL) was added trimethylsilyldiazomethane (12.1 ml of a 2M solution in hexanes, 24.4 mmol) and the mixture was stirred for 16 hr at rt. Additional trimethylsilyldiazomethane (24.0 ml of a 2M solution in hexanes, 48 mmol) was added and the reaction was stirred for 16 hr. The reaction was quenched by the addition of acetic acid (2 mL) and the solvent was evaporated in vacuo. The residue was purified by flash chromatography eluting with MeOH/CH2Cl2 (5-15% gradient elution), to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-15e572bf5d014ef2bc44b7f7af929762
Source noteuspto-grants-2005_07