HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790459Generated: October 31, 2026
Isopropylamine → 1-[1-(4-Fluorophenethyl)-piperdin-4-yl]-6-(isopropylcarbamoylmethyl)indoline
https://huagongshe.com/reaction/1790459
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-carboxymethylindoline | HCID 22038043 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[1-(4-Fluorophenethyl)-piperdin-4-yl]-6-(isopropylcarbamoylmethyl)indoline | HCID 22037974 | 52% |
Reaction Steps
Under ice cooling, 1,1′-carbonyldimidazole (15 g) was added to a solution of 1-[1-(4-fluorophenethyl)piperidin-4-yl]-6-carboxymethylindoline (30 g) in dimethylformamide (240 ml) and the resultant mixture was stirred for 2 hr. After adding isopropylamine (5.6 g), the mixture was warmed to room temperature and then stirred for additional 2 hr. Next, ice water (240 ml) and ethyl acetate (300 ml) were added to the reaction solution and the layers were separated. The organic layer was washed successively with water, a saturated aqueous solution of sodium bicarbonate and brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in hot ethyl acetate (80 ml). After allowing to cool to room temperature, the resulting crystals were collected by filtration to give the title compound (17.2 g) as a white powder (yield: 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071201B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-1cb140fd327d45739df3badf916eff95 |
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| Source note | uspto-grants-2006_07 |
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