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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219633Generated: October 30, 2026

N-[bis(methylsulfanyl)methylidene]methanesulfonamide → HCID 178504234, compound

https://huagongshe.com/reaction/2219633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[bis(methylsulfanyl)methylidene]methanesulfonamideHCID 13449843—
Reactant4-Cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [4-(2-amino-1-aminomethyl-ethyl)-2-cyclohex-1-enyl-phenyl]-amideHCID 59771233—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178504234HCID 17850423439%

Reaction Steps

A solution of 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [4-(2-amino-1-aminomethyl-ethyl)-2-cyclohex-1-enyl-phenyl]-amide (as prepared in Example 12, step (d), 250 mg, 0.506 mmol) and N-(bis-methylsulfanyl-methylene)-methanesulfonamide (Australian Journal of Chemistry, 46(6), 873, (1993), 100 mg, 0.506 mmol) in 1,2-dichloroethane (20 mL) was heated at reflux for 4 h. The reaction mixture was concentrated, and the residue was purified on silica (20-100% EtOAc-hexane) to obtain the title compound (117 mg, 39%): Mass spectrum, (ESI, m/z): Calcd. for C28H39N7O4SSi, 598.2 (M+H). found 598.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414050B2
Source datasetuspto-grants-2008_08
ORD IDord-8455d7501ba04d8bb73e5cbeb00a6db3
Source noteuspto-grants-2008_08