Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Nitrogen mustard hydrochloride | HCID 5935 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Acetyl-6-aminoindoline | HCID 258564 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 22118897 | HCID 22118897 | 22% |
Reaction Steps
A stirred mixture of 1-acetyl-6-amino-2,3-dihydro-1H-indole (D10, 37.8 g, 0.22 mole), mechlorethamine hydrochloride (46 g, 0.24 mole) and anhydrous potassium carbonate (80 g, 0.58 mole) in 1-butanol (1800 ml) was heated at reflux for 8 h, then additional mechlorethamine hydrochloride (25 g, 0.13 mole) and potassium carbonate (41 g, 0.30 mole) were added and reflux continued for 3 h. The reaction mixture was allowed to cool and then washed with water (1000 ml). The aqueous wash was extracted with ethyl acetate, and the extract combined with the 1-butanol solution and concentrated in vacuo. The brown oily residue (60 g) was chromatographed on silica gel eluting with 0-8% MeOH/DCM to give an orange oil, which was trituated with ether to afford the title compound as a beige solid (12.2 g, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06159979 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-5ca54176b2bc44b1ae9710bffdc3b2b9 |
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| Source note | uspto-grants-2000_12 |
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