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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Bis(2,2-dimethylpropoxy)-N,N-dimethylmethanamine | HCID 78623 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68766702 | HCID 68766702 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23139275 | HCID 23139275 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829580B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-556fcf7ac9784c5a8a36929f499ebee1 |
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| Source note | uspto-grants-2010_11 |
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