HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843939Generated: October 29, 2026
Potassium Carbonate → 6-benzyloxy-3-(propyl)amino-1,2,3,4-tetrahydro-9H-carbazole
https://huagongshe.com/reaction/843939
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazole | HCID 22611308 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-benzyloxy-3-(propyl)amino-1,2,3,4-tetrahydro-9H-carbazole | HCID 22611390 | 39.4% |
Reaction Steps
To a solution of 0.600 gm (2.05 mMol) 6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazole in 35 mL acetonitrile were added 0.283 gm (2.05 mMol) potassium carbonate followed by 240 μL (2.46 mMol) iodopropane and the reaction mixture was stirred at room temperature for 2.5 days. Additional iodopropane was added and the reaction stirred at room temperature until all of the starting material had been consumed. The reaction mixture was then partitioned between dichloromethane and water. The aqueous phase was extracted with dichloromethane and the combined organic phases were then dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 96.5:3:0.5 dichloromethane: isopropanol:ammonium hydroxide. Fractions shown to contain the desired compound were concentrated under reduced pressure to give 0.270 gm (39%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380201B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-2a44b651a3d54f439bfa68543c8574c7 |
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| Source note | uspto-grants-2002_04 |
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