Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 5-Fluoro-2-nitroaniline | HCID 75399 | — |
| Reactant | HCID 58650608 | HCID 58650608 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58650614 | HCID 58650614 | — |
Reaction Steps
A mixture of 5-fluoro-2-nitroaniline (1.1 equivalents), [((2S,5S)-5-methylmorpholin-2-yl)methyl]dimethylamine (1 equivalent), triethylamine (3 equivalents), and N-methylpyrrolidinone was heated at 140° C. for 48 hours in a sealed high pressure vessel. The reaction mixture was then cooled to 25° C. and dissolved in CH2Cl2. The solution was washed with water (×2) and dried over Na2SO4. Purification via chromatography on silica gel (10% MeOH in dichloromethane) afforded the desired product as a dark yellow foam. LC/MS (m/z) 295.2 (MH+) Rt 1.55 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07064215B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-0a5a3bfdb8654bb886d8b1abb7ca6a13 |
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| Source note | uspto-grants-2006_06 |
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