Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754960Generated: October 28, 2026

Ethane, 2-bromo-1,1-diethoxy- → HCID 66816955, compound

https://huagongshe.com/reaction/1754960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantHCID 86672764HCID 86672764—
SolventAcetic AcidHCID 176—
ProductHCID 66816955HCID 668169556.8%

Reaction Steps

Bromoacetaldehyde diethylacetal (44.2 mg, 0.224 mmol) was added to a solution of 1-(3,5-dimethyl-4-{2-[2-(4-methyl-cyclohexyl)-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-ene-8-sulfonyl]-ethyl}-phenyl)-1-methyl-thiourea (100 mg, 0.187 mmol) in acetic acid (2 ml) in a nitrogen stream. The mixture was heated under reflux for two hours and then concentrated under reduced pressure. The resulting residue was diluted with dichloromethane, and the organic layer was then sequentially washed with a saturated aqueous sodium bicarbonate solution and saturated brine and dried over anhydrous magnesium sulfate. The organic layer was concentrated, and the resulting residue was then purified by silica gel column chromatography (dichloromethane-methanol) to give 8-{2-[2,6-Dimethyl-4-(methyl-thiazol-2-yl-amino)-phenyl]-ethanesulfonyl}-2-(4-methyl-cyclohexyl)-1,3,8-triaza-spiro[4.5]dec-1-en-4-one (7.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-a50678a31f024377980bcba6eb58f452
Source noteuspto-grants-2015_10