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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694508Generated: October 25, 2026

Phenylsilane → 5-Cyclohex-1-enyl-3-(4-[1,2,4]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1694508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylsilaneHCID 12752—
Reactant4-[1,2,4]Triazol-1-yl-cyclohexanoneHCID 57424093—
Reactant5-Cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl esterHCID 57795401—
CatalystDibutyltin dichlorideHCID 12688—
Product5-Cyclohex-1-enyl-3-(4-[1,2,4]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl esterHCID 5779542792.6%

Reaction Steps

A mixture of intermediate 1, 4-[1,2,4]triazol-1-yl-cyclohexanone (257 mg, 1.55 mmol) and 3-Amino-5-cyclohex-1-enyl-thiophene-2-carboxylic acid methyl ester (compound x, see Irina) (368 mg, 1.55 mmol) was treated by dibutyltin dichloride (24 mg, 0.078 mmol). The resulting mixture was stirred 5 min at room temperature and phenylsilane (210 μl, 1.70 mmol) was added. The reaction mixture was stirred at room temperature under nitrogen for 40 h. Solvent was removed and the crude was purified by silica gel column chromatography using a gradient from 50% EtOAc:hexanes to 100% EtOAc as eluent to give 5-cyclohex-1-enyl-3-(4-[1,2,4]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl ester (555 mg, 92%) as a yellow mixture of cis and trans isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158675B2
Source datasetuspto-grants-2012_04
ORD IDord-0c027492b19643cc8fbe8b6ea1ebf551
Source noteuspto-grants-2012_04