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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340559Generated: October 26, 2026

4-Cyano-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carboxylic acid → Acetic acid 3-acetoxy-2-(4-{[4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carbonyl]-amino}-3-cyclohex-1-enyl-phenyl)-propyl ester

https://huagongshe.com/reaction/340559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyano-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carboxylic acidHCID 59128585—
ReactantAcetic acid 3-acetoxy-2-(4-amino-3-cyclohex-1-enyl-phenyl)-propyl esterHCID 59771138—
Reactantpotassium 4-cyano-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carboxylateHCID 67188357—
ProductAcetic acid 3-acetoxy-2-(4-{[4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carbonyl]-amino}-3-cyclohex-1-enyl-phenyl)-propyl esterHCID 59771165—

Reaction Steps

Acetic acid 3-acetoxy-2-(4-amino-3-cyclohex-1-enyl-phenyl)-propyl ester (as prepared in the previous step) was coupled to 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid, potassium salt (as prepared in Example 1, step (d)) as described in Example 1, step (1) to obtain the title compound: Mass spectrum (ESI, m/z): Calcd. for C30H40N4O6Si, 581.2 (M+H). found 581.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895584B2
Source datasetuspto-grants-2014_11
ORD IDord-fb9fd90e47734713896c34f61a2ad43e
Source noteuspto-grants-2014_11