Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Benzene, 1-isocyanato-4-nitro- | HCID 66012 | — |
| Reactant | Methyl 2-amino-4-[(tert-butoxycarbonyl)amino]benzoate | HCID 21056495 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21951863 | HCID 21951863 | 47.2% |
Reaction Steps
A solution of 2-amino-4-(tert-butoxycarbonylamino)-benzoic acid methyl ester (6.3 g, 23.6 mmol) and 4-nitrophenyl isocyanate (7.8 g, 47.4 mmoles) in 100 mL dry dimethylformamide was stirred at room temperature for 20 hrs. To it was then added diisopropylamine (8.2 mL, 47.4 mmol), and the reaction mixture was heated in 80° C. bath for 2 hrs. It was cooled to room temperature and the solid precipitates were filtered off. The dimethylformamide filtrate was concentrated in vacuo to evaporate the solvent. To the residue was added 400 mL dichloromethane. After stirred and swirled, the solid was isolated by filtration. This solid was then dissolved in 100 mL dimethylformamide and 200 mL methanol. To it was added 1.0 g 10% Pd/C, and the mixture was subjected to standard hydrogenation using a balloon for 20 hrs. It was filtered through a celite bed. The filtrate was concentrated in vacuo and purified using flash column to afford the title compound (4.1 g, 44%). ES+ MS showed 397 m/z, the correct mass for the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109332B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-7b59d108aac445f49dbbb089cdb00bd4 |
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| Source note | uspto-grants-2006_09 |
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