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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171652Generated: November 1, 2026

1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamine → HCID 23139275, compound

https://huagongshe.com/reaction/1171652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamineHCID 78623—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68766702HCID 68766702—
ReactantHCID 178418634HCID 178418634—
SolventTolueneHCID 1140—
ProductHCID 23139275HCID 2313927538%

Reaction Steps

To a solution of (E)-3-{[1-(t-butoxycarbonyl)indol-3-yl]methylidene}-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]piperidin-4-ol (1.58 g) in toluene (32 ml) were added thioacetic acid (0.45 ml) and N,N-dimethylformamide dineopentyl acetal (1.75 ml) under ice-cooling, and the resulting mixture was stirred at room temperature for 1 hour. After stirring, to the reaction mixture was added saturated aqueous sodium hydrogencarbonate solution, and the resulting mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution, and the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:9) as the eluent to afford (E)-4-(acetylsulfanyl)-3-{[1-(t-butoxycarbonyl)indol-3-yl]methylidene}-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]piperidine (0.66 g, yield: 38%) as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-556fcf7ac9784c5a8a36929f499ebee1
Source noteuspto-grants-2010_11