Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 3-Nitro-4-(trifluoromethoxy)aniline | HCID 613694 | — |
| Reactant | HCID 43725938 | HCID 43725938 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23110306 | HCID 23110306 | — |
Reaction Steps
29 g (146.5 mmol) diphosgene in 300 ml 1,2-dichlorethane were treated at −20° C. with a solution of 13 g (58.6 mmol) 3-nitro-4-(trifluormethoxy)-aniline in 20 ml 1,2-dichlorethane. The mixture was allowed to come to room temperature and then was heated to 50° C. for 3 h. After standing over night, the solvent was evaporated and the residual oil was taken up in 250 ml THF. 13 g (58.6 mmol) 2-methyl-2-[(pyridin-4-ylmethyl)-amino]-propionic acid methyl ester in 250 ml THF were added and the mixture was heated to 40° C. for 1 h. The solvent was evaporated and the residue purified by flash chromatography (Silica gel, methylene chloride:methanol=95:5). Yield: 19.7 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759379B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-38df5afa8d954ccfba6e0b8223518c69 |
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| Source note | uspto-grants-2010_07 |
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