Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711301Generated: October 25, 2026

Diisopropylethylamine → 4-Cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [2-(4,4-dimethyl-cyclohex-1-enyl)-4-(6-methoxy-pyridin-3-yl)-phenyl]-amide

https://huagongshe.com/reaction/1711301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBroPHCID 2733179—
Reactant2-(4,4-Dimethyl-cyclohex-1-enyl)4-(6-methoxy-pyridin-3-yl)-phenylamineHCID 58754885—
Reactantpotassium 4-cyano-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carboxylateHCID 67188357—
Product4-Cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [2-(4,4-dimethyl-cyclohex-1-enyl)-4-(6-methoxy-pyridin-3-yl)-phenyl]-amideHCID 58754867—

Reaction Steps

The title compound was prepared from 2-(4,4-dimethyl-cyclohex-1-enyl)4-(6-methoxy-pyridin-3-yl)-phenylamine (as prepared in the previous step, 16.4 mg, 0.0530 mmol), potassium 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylate (as prepared in Example 11, step (d), 23 mg, 0.074 mmol), PyBroP (40 mg, 0.084 mmol) and DIEA (23 μL, 0.13 mmol) according to the procedure in Example 11, step (f) (20 mg, 68%). Mass spectrum (ESI, m/z): Calcd. for C31H39N5O3Si, 558.2 (M+H), found 558.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-65cd7e613e7c44019e1b62c039fc6f62
Source noteuspto-grants-2010_09