Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 56993864 | HCID 56993864 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54370181 | HCID 54370181 | — |
Reaction Steps
3.4 g (8.5 mmol) of dimethyl (R)-N-(7-nitro-2,3-dimethoxyquinoxalin-5-ylmethyl)-α-aminoethylphosphonate, 8.9 ml (7.5 eq.) of ethyl iodide and 20.9 ml (14.5 eq.) of Hunig's base are mixed in 18 ml of acetonitrile and stirred at 55° C. for 18 hours. The reaction mixture is evaporated and slurried with ethyl acetate. The deposited solid is filtered off and washed with ethyl acetate. The title compound is obtained in the form of a yellow resin after evaporation of the filtrate and column chromatography using ethyl acetate/methanol (95:5) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06117873 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-7a0a108403ab4f1c9a76169b921e4892 |
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| Source note | uspto-grants-2000_09 |
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