Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099679Generated: October 26, 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/2099679

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 numberUS07569600B2
Source datasetuspto-grants-2009_08
ORD IDord-24d5ce1749444f3a98ac4eb4c9c4dd91
Source noteuspto-grants-2009_08