Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-2,4-difluoro-5-nitrobenzoic acid | HCID 15549918 | — |
| Catalyst | Methylamine | HCID 6329 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57855931 | HCID 57855931 | 102.2% |
Reaction Steps
A suspension of 5 g (21.05 mmol) of 3-chloro-2,4-difluoro-5-nitro-benzoic acid (known from WO 03/077914) in 50 mL of H2O is cooled to a temperature of 0° C. Then 5.86 ml (42.10 mmol) of triethylamine were added dropwise followed by the dropwise addition of 1.82 ml (21.05 mmol) of methylamine (40% in H2O). After 30 min of stirring at 0° C., 0.18 ml (2.11 mmol) of methylamine (40% in H2O) is added and the mixture is stirred again during 30 min at a temperature of 0° C. The pH of the mixture is adjusted to 1-0.5 by the addition of concentrated HCl at a temperature of 0° C. The product is extracted with tert-butyl methyl ether (2 times) and the organic phase is washed once with brine, dried on Na2SO4, filtrated and the solvent is evaporated. 5.35 g (21.52 mmol, 102%) of a crude yellow solid were obtained and used directly in the next step without purification. LC/MS: 247/249 (M−1)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08580785B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-c6e2d1c1f97d4b8bb389489de4a9808b |
|---|
| Source note | uspto-grants-2013_11 |
|---|