HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506644Generated: November 1, 2026
Acetic Acid → 8-(1-(cyclopropylmethyl)piperidin-4-yloxy)-3,4-dihydropyrazino[1,2-a]indol-1(2H)-one
https://huagongshe.com/reaction/506644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 8-(Piperidin-4-yloxy)-3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one | HCID 68461083 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(1-(cyclopropylmethyl)piperidin-4-yloxy)-3,4-dihydropyrazino[1,2-a]indol-1(2H)-one | HCID 16679520 | 30% |
Reaction Steps
To the solution of 0.27 g (0.95 mmol) 8-(piperidin-4-yloxy)-3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one in 6 mL tetrahydrofuran, 20 μL water, 11 μL (99 μg, 1.42 mmol) cyclopropanecarboxaldehyde, 0.16 mL (0.17 g, 2.8 mmol) acetic acid and 1.42 mL (1.42 mmol, 1M solution in tetrahydrofuran) sodium cyanoborohydride were added and the reaction mixture was stirred for 18 hours at 55° C. The mixture was poured on 10% aqueous sodium bicarbonate and was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed on silica gel with dichloromethane: methanol:ammonia (9:1:0.1 v/v) as eluant to give 96 μg (30%) of the desired compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786109B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-1f92fa6bbe804a9c918f00bda966e38f |
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| Source note | uspto-grants-2010_08 |
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