HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726002Generated: October 30, 2026
N-Carbethoxyphthalimide → HCID 22611405, compound
https://huagongshe.com/reaction/726002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | 3-(1-Methylpiperidin-4-yl)-1h-indol-5-amine | HCID 11831220 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 22611405 | HCID 22611405 | 65% |
Reaction Steps
To a solution of 0.458 gm (2.0 mMol) 5-amino-3-(1-methylpiperidin-4-yl)-1H-indole in 8.0 mL dichloromethane were added 0.438 gm (2.0 mMol) N-carbethoxyphthalimide. The reaction mixture was stirred 18 hours at ambient temperature, at which time the solvent was removed under reduced pressure. The residue was subjected to flash chromatography, eluting with 100:20:0.5 dichloromethane:methanol:ammonium hydroxide, giving 0.467 gm (65%) of 5-phthalimido-3-(1-methylpiperidin-4-yl)-1H-indole as a yellow foam. The yellow foam was dissolved in a mixture of methanol:ethyl acetate and to it was added an equivalent of oxalic acid. The colorless precipitate which formed was recrystallized from methanol to give 0.267 gm of the title compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05708008 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-91ee40fe432746d5b912cadef88ffd96 |
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| Source note | uspto-grants-1998_01 |
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